2-Oxo-2H-chromen-4-yl 4-ethyl­benzoate

Valentin Bationo; Abel Landry Tebily; Akoun Abou; Charles Bavouma Sombié; Rasmané Semdé; Abdoulaye Djandé

doi:10.1107/S2414314625007345

. 2025 Aug 19;10(Pt 8):x250734. doi: 10.1107/S2414314625007345

2-Oxo-2H-chromen-4-yl 4-ethylbenzoate

Valentin Bationo ^a, Abel Landry Tebily ^b, Akoun Abou ^b,^*, Charles Bavouma Sombié ^c, Rasmané Semdé ^c, Abdoulaye Djandé ^a

Editor: W T A Harrison^d

PMCID: PMC12412682 PMID: 40917538

In the title compound, the dihedral angle between the coumarin ring system and the phenyl ring is 63.46 (5)°. In the crystal, the molecules are linked by weak C—H⋯O hydrogen bonds and aromatic π–π stacking interactions

Keywords: crystal structure, hydrogen bonding, π–π stacking, centrosymmetric dimer

Abstract

In the title compound, C₁₈H₁₄O₄, the dihedral angle between the coumarin moiety and the phenyl fragment is 63.46 (5)°. In the crystal, the molecules are linked by weak C—H⋯O hydrogen bonds and aromatic π–π stacking interactions. A short C=O⋯π [O⋯π = 3.2667 (10) Å] contact is also observed.

Structure description

Coumarins are a broad class of over 800 naturally occurring chemicals and are frequently found in plants like sweet clover and tonka beans (Ziarani et al., 2018 ▸). Some coumarins have therapeutic potential due to their wide range of biological activities (Akkol et al. 2020 ▸) such as anti-inflammatory action (Tuan Anh et al., 2017 ▸; Tosun et al., 2009 ▸). As part of our work in this area, we now describe the synthesis and structure of the title compound (I).

As expected, the C1–C9/O1 coumarin ring system in (I) (Fig. 1 ▸) is almost planar (r.m.s deviation = 0.004 Å) and is oriented at an angle of 63.46 (5)° with respect to the C11–C16 ring. Atom C18 lies close to the latter ring plane [deviation = −0.166 (1) Å]. The pyrone ring shows the usual asymmetric bond lengths for C3—C2 [1.3443 (15) Å] and C2—C1 [1.4508 (15) Å], which are shorter and longer, respectively, than would be expected for a C_ar—C_ar bond (Gomes et al., 2016 ▸; Koulabiga et al., 2024 ▸).

The molecular structure of (I) with displacement ellipsoids drawn at the 50% probability level.

In the extended structure of (I) (Figs. 2 ▸ and 3 ▸), the molecules are linked by weak C—H⋯O hydrogen bonds (Table 1 ▸). The C2—H2⋯O2 interaction results in the formation of inversion dimers, which are characterized by an Inline graphic (8) graph-set motif. Subsequently, these dimers combine with the C9—H9⋯O4 and C16—H16⋯O2 hydrogen bonds to form an (16) graph-set motif. An aromatic π–π stacking interaction is observed between the C1–C5/O1 and C4–C9 rings [centroid–centroid separation = 3.6514 (7) Å, slippage = 1.613 Å] and a short C=O⋯π contact of 3.2667 (10) Å occurs (Table 1 ▸).

A view of the crystal packing of (I), showing C=O⋯π and π–π stacking interactions (dashed lines). The green dots are centroids of rings.

Detail of the packing of (I) showing the association of molecules into centrosymmetric dimers through pairwise C—H⋯O hydrogen bonds. This generates (8) and (16) graph-set motifs that extend along the a-axis direction. H atoms not involved in hydrogen bonding have been omitted for clarity.

Inline graphic — Detail of the packing of (I) showing the association of molecules into centrosymmetric dimers through pairwise C—H⋯O hydrogen bonds. This generates (8) and (16) graph-set motifs that extend along the a-axis direction. H atoms not involved in hydrogen bonding have been omitted for clarity.

Table 1. Hydrogen-bond geometry (Å, °).

Cg1 is the centroid of the C1–C5/O1 ring.

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C2—H2⋯O2ⁱ	0.93	2.49	3.4223 (14)	176
C9—H9⋯O4ⁱⁱ	0.93	2.57	3.4164 (14)	151
C16—H16⋯O2ⁱⁱⁱ	0.93	2.54	3.4436 (14)	163
C1—O2⋯Cg1^iv	1.22 (1)	3.27 (1)	3.5408 (14)	93 (1)

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Symmetry codes: (i) Inline graphic ; (ii) ; (iii) ; (iv) .

Synthesis and crystallization

To a solution of 4-ethylbenzoyl chloride (0.95 ml, 6.2 mmol, 1 equiv.) in dried tetrahydrofuran (30 ml) was added dried triethylamine (2.6 ml, 3 equiv.) and 4-hydroxycoumarin (1.00 g, 6.17 mmol, 1 equiv.) in small portions over 30 min. The mixture was then refluxed for 4 h under stirring and poured into 40 ml of chloroform. The solution was acidified with dilute hydrochloric acid until its discoloration. The organic layer was extracted, concentrated in a vacuum until a slight cloudiness was obtained and then cooled in an ice bath. The resulting precipitate was filtered off with suction, washed with petroleum ether and recrystallized from a chloroform–hexane solvent mixture (1:3) giving the title compound (1.12 g, yield 68%, m.p. 459–461 K). Colorless prisms appropriate for single-crystal X-ray diffraction analysis were obtained by slow evaporation of an acetone solution.

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸.

Table 2. Experimental details.

Crystal data
Chemical formula	C₁₈H₁₄O₄
M _r	294.29
Crystal system, space group	Triclinic, P
Temperature (K)	296
a, b, c (Å)	4.2781 (4), 10.7096 (9), 15.3525 (13)
α, β, γ (°)	84.816 (3), 86.728 (3), 83.925 (3)
V (Å³)	695.79 (11)
Z	2
Radiation type	Mo Kα
μ (mm⁻¹)	0.10
Crystal size (mm)	0.33 × 0.16 × 0.07

Data collection
Diffractometer	SuperNova, Dual, Cu at home/near, AtlasS2
Absorption correction	Multi-scan (CrysAlis PRO; Rigaku OD, 2022 ▸)
T_min, T_max	0.956, 1.000
No. of measured, independent and observed [I > 2σ(I)] reflections	59779, 4332, 3675
R _int	0.037
(sin θ/λ)_max (Å⁻¹)	0.721

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.049, 0.144, 1.11
No. of reflections	4332
No. of parameters	200
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.32, −0.28

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Computer programs: CrysAlis PRO (Rigaku OD, 2022 ▸), SHELXT2018/2 (Sheldrick, 2015a ▸), PLATON (Spek, 2020 ▸) and WinGX (Farrugia, 2012 ▸), SHELXL2018/3 (Sheldrick, 2015b ▸) and publCIF (Westrip, 2010 ▸).

Supplementary Material

Crystal structure: contains datablock(s) I. DOI: 10.1107/S2414314625007345/hb4531sup1.cif

x-10-x250734-sup1.cif^{(1.7MB, cif)}

Structure factors: contains datablock(s) I. DOI: 10.1107/S2414314625007345/hb4531Isup3.hkl

x-10-x250734-Isup3.hkl^{(345KB, hkl)}

x-10-x250734-Isup3.cml^{(5.6KB, cml)}

Supporting information file. DOI: 10.1107/S2414314625007345/hb4531Isup3.cml

CCDC reference: 2481234

Additional supporting information: crystallographic information; 3D view; checkCIF report

Acknowledgments

The authors thank the Institute Jean Barriol (Université de Lorraine, France) for the X-ray diffraction measurements.

full crystallographic data

2-Oxo-2H-chromen-4-yl 4-ethylbenzoate . Crystal data

C₁₈H₁₄O₄	F(000) = 308
M_r = 294.29	D_x = 1.405 Mg m⁻³
Triclinic, P1	Melting point = 459–461 K
a = 4.2781 (4) Å	Mo Kα radiation, λ = 0.71073 Å
b = 10.7096 (9) Å	Cell parameters from 4332 reflections
c = 15.3525 (13) Å	θ = 4.5–61.7°
α = 84.816 (3)°	µ = 0.10 mm⁻¹
β = 86.728 (3)°	T = 296 K
γ = 83.925 (3)°	Prism, colorless
V = 695.79 (11) Å³	0.33 × 0.16 × 0.07 mm
Z = 2

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2-Oxo-2H-chromen-4-yl 4-ethylbenzoate . Data collection

SuperNova, Dual, Cu at home/near, AtlasS2 diffractometer	4332 independent reflections
Radiation source: micro-focus sealed X-ray tube	3675 reflections with I > 2σ(I)
Detector resolution: 5.3048 pixels mm^-1	R_int = 0.037
ω scans	θ_max = 30.8°, θ_min = 2.2°
Absorption correction: multi-scan (CrysAlisPro; Rigaku OD, 2022)	h = −6→6
T_min = 0.956, T_max = 1.000	k = −15→15
59779 measured reflections	l = −22→22

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2-Oxo-2H-chromen-4-yl 4-ethylbenzoate . Refinement

Refinement on F²	Hydrogen site location: inferred from neighbouring sites
Least-squares matrix: full	H-atom parameters constrained
R[F² > 2σ(F²)] = 0.049	w = 1/[σ²(F_o²) + (0.0753P)² + 0.2292P] where P = (F_o² + 2F_c²)/3
wR(F²) = 0.144	(Δ/σ)_max < 0.001
S = 1.11	Δρ_max = 0.32 e Å⁻³
4332 reflections	Δρ_min = −0.28 e Å⁻³
200 parameters	Extinction correction: SHELXL2018/3 (Sheldrick, 2015b), Fc^*=kFc[1+0.001xFc²λ³/sin(2θ)]^-1/4
0 restraints	Extinction coefficient: 0.016 (6)
Primary atom site location: structure-invariant direct methods

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2-Oxo-2H-chromen-4-yl 4-ethylbenzoate . Special details

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Refinement. The H atoms were placed at calculated positions [C—H = 0.93–0.97 Å] and refined using the riding model approximation with U_iso(H) = 1.2U_eq(C) or 1.5U_eq(methyl C).

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2-Oxo-2H-chromen-4-yl 4-ethylbenzoate . Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²)

	x	y	z	U_iso*/U_eq
O1	1.33648 (19)	0.16608 (7)	0.02913 (5)	0.02074 (17)
O3	0.87511 (19)	0.43581 (7)	0.18225 (5)	0.02160 (18)
O2	1.5944 (2)	0.31182 (8)	−0.04602 (5)	0.0267 (2)
O4	1.1515 (2)	0.36404 (8)	0.30123 (5)	0.02480 (19)
C11	0.7673 (2)	0.54303 (9)	0.30997 (7)	0.0195 (2)
C3	1.0391 (3)	0.34377 (10)	0.13411 (7)	0.0193 (2)
C5	1.1274 (2)	0.12891 (10)	0.09534 (7)	0.0187 (2)
C10	0.9530 (2)	0.43848 (10)	0.26765 (7)	0.0194 (2)
C2	1.2424 (3)	0.38058 (10)	0.06923 (7)	0.0215 (2)
H2	1.280225	0.464811	0.060129	0.026*
C14	0.4429 (3)	0.73961 (10)	0.39781 (7)	0.0207 (2)
C4	0.9691 (2)	0.21466 (9)	0.15046 (7)	0.0190 (2)
C7	0.8695 (3)	−0.03992 (10)	0.16993 (7)	0.0232 (2)
H7	0.834208	−0.124535	0.176664	0.028*
C13	0.6335 (3)	0.64501 (11)	0.44302 (7)	0.0242 (2)
H13	0.652704	0.646856	0.502909	0.029*
C6	1.0813 (3)	0.00155 (10)	0.10473 (7)	0.0209 (2)
H6	1.190075	−0.054437	0.068072	0.025*
C17	0.2679 (3)	0.84887 (10)	0.44238 (8)	0.0251 (2)
H17A	0.050253	0.857056	0.426309	0.030*
H17B	0.356950	0.925553	0.419603	0.030*
C15	0.4150 (3)	0.73322 (10)	0.30800 (7)	0.0230 (2)
H15	0.287568	0.795705	0.277112	0.028*
C16	0.5729 (3)	0.63586 (10)	0.26384 (7)	0.0214 (2)
H16	0.549281	0.632588	0.204266	0.026*
C1	1.4032 (3)	0.28936 (10)	0.01336 (7)	0.0211 (2)
C12	0.7957 (3)	0.54759 (10)	0.39939 (7)	0.0243 (2)
H12	0.923771	0.485241	0.430213	0.029*
C9	0.7567 (3)	0.17035 (10)	0.21634 (7)	0.0214 (2)
H9	0.648923	0.225798	0.253545	0.026*
C8	0.7082 (3)	0.04399 (11)	0.22575 (7)	0.0239 (2)
H8	0.567671	0.014693	0.269405	0.029*
C18	0.2734 (3)	0.83910 (12)	0.54170 (8)	0.0312 (3)
H18A	0.156830	0.912340	0.563515	0.047*
H18B	0.179577	0.765055	0.565512	0.047*
H18C	0.487067	0.833730	0.558788	0.047*

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2-Oxo-2H-chromen-4-yl 4-ethylbenzoate . Atomic displacement parameters (Å²)

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
O1	0.0244 (4)	0.0187 (3)	0.0191 (4)	−0.0020 (3)	0.0021 (3)	−0.0037 (3)
O3	0.0271 (4)	0.0181 (3)	0.0193 (4)	0.0023 (3)	−0.0017 (3)	−0.0051 (3)
O2	0.0312 (4)	0.0266 (4)	0.0220 (4)	−0.0046 (3)	0.0046 (3)	−0.0019 (3)
O4	0.0271 (4)	0.0226 (4)	0.0243 (4)	0.0039 (3)	−0.0043 (3)	−0.0053 (3)
C11	0.0217 (5)	0.0159 (4)	0.0211 (5)	−0.0017 (3)	−0.0009 (4)	−0.0030 (3)
C3	0.0222 (5)	0.0175 (4)	0.0180 (4)	0.0011 (3)	−0.0030 (3)	−0.0038 (3)
C5	0.0196 (4)	0.0188 (4)	0.0177 (4)	−0.0009 (3)	−0.0013 (3)	−0.0023 (3)
C10	0.0218 (5)	0.0176 (4)	0.0191 (4)	−0.0025 (3)	−0.0008 (3)	−0.0029 (3)
C2	0.0260 (5)	0.0180 (4)	0.0207 (5)	−0.0026 (4)	−0.0020 (4)	−0.0023 (3)
C14	0.0228 (5)	0.0164 (4)	0.0231 (5)	−0.0024 (4)	0.0008 (4)	−0.0028 (3)
C4	0.0205 (5)	0.0179 (4)	0.0185 (4)	−0.0008 (3)	−0.0022 (3)	−0.0025 (3)
C7	0.0262 (5)	0.0187 (4)	0.0248 (5)	−0.0034 (4)	−0.0041 (4)	0.0002 (4)
C13	0.0289 (5)	0.0221 (5)	0.0215 (5)	0.0023 (4)	−0.0032 (4)	−0.0057 (4)
C6	0.0232 (5)	0.0173 (4)	0.0223 (5)	−0.0001 (4)	−0.0033 (4)	−0.0036 (3)
C17	0.0292 (6)	0.0182 (5)	0.0271 (5)	0.0011 (4)	0.0019 (4)	−0.0042 (4)
C15	0.0277 (5)	0.0169 (4)	0.0235 (5)	0.0010 (4)	−0.0018 (4)	−0.0009 (4)
C16	0.0265 (5)	0.0183 (4)	0.0193 (4)	−0.0013 (4)	−0.0012 (4)	−0.0015 (3)
C1	0.0239 (5)	0.0200 (5)	0.0192 (4)	−0.0022 (4)	−0.0016 (4)	−0.0012 (3)
C12	0.0289 (5)	0.0205 (5)	0.0230 (5)	0.0037 (4)	−0.0046 (4)	−0.0041 (4)
C9	0.0220 (5)	0.0222 (5)	0.0200 (5)	−0.0018 (4)	−0.0006 (4)	−0.0027 (4)
C8	0.0249 (5)	0.0249 (5)	0.0221 (5)	−0.0057 (4)	−0.0012 (4)	0.0004 (4)
C18	0.0400 (7)	0.0250 (5)	0.0277 (6)	0.0048 (5)	0.0022 (5)	−0.0085 (4)

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2-Oxo-2H-chromen-4-yl 4-ethylbenzoate . Geometric parameters (Å, º)

O1—C5	1.3750 (13)	C7—C6	1.3861 (15)
O1—C1	1.3775 (13)	C7—C8	1.3995 (16)
O3—C10	1.3747 (13)	C7—H7	0.9300
O3—C3	1.3915 (12)	C13—C12	1.3924 (15)
O2—C1	1.2146 (13)	C13—H13	0.9300
O4—C10	1.2062 (13)	C6—H6	0.9300
C11—C12	1.3908 (15)	C17—C18	1.5202 (17)
C11—C16	1.3954 (15)	C17—H17A	0.9700
C11—C10	1.4802 (14)	C17—H17B	0.9700
C3—C2	1.3443 (15)	C15—C16	1.3891 (15)
C3—C4	1.4425 (14)	C15—H15	0.9300
C5—C6	1.3922 (14)	C16—H16	0.9300
C5—C4	1.4004 (14)	C12—H12	0.9300
C2—C1	1.4508 (15)	C9—C8	1.3842 (15)
C2—H2	0.9300	C9—H9	0.9300
C14—C13	1.3912 (15)	C8—H8	0.9300
C14—C15	1.3991 (15)	C18—H18A	0.9600
C14—C17	1.5161 (15)	C18—H18B	0.9600
C4—C9	1.4047 (15)	C18—H18C	0.9600

C5—O1—C1	122.05 (8)	C5—C6—H6	120.7
C10—O3—C3	117.26 (8)	C14—C17—C18	115.86 (9)
C12—C11—C16	119.86 (10)	C14—C17—H17A	108.3
C12—C11—C10	117.31 (9)	C18—C17—H17A	108.3
C16—C11—C10	122.83 (9)	C14—C17—H17B	108.3
C2—C3—O3	118.14 (9)	C18—C17—H17B	108.3
C2—C3—C4	122.17 (9)	H17A—C17—H17B	107.4
O3—C3—C4	119.51 (9)	C16—C15—C14	121.64 (10)
O1—C5—C6	116.49 (9)	C16—C15—H15	119.2
O1—C5—C4	121.75 (9)	C14—C15—H15	119.2
C6—C5—C4	121.75 (10)	C15—C16—C11	119.17 (10)
O4—C10—O3	122.50 (9)	C15—C16—H16	120.4
O4—C10—C11	126.07 (10)	C11—C16—H16	120.4
O3—C10—C11	111.42 (9)	O2—C1—O1	116.76 (10)
C3—C2—C1	120.23 (10)	O2—C1—C2	125.71 (10)
C3—C2—H2	119.9	O1—C1—C2	117.53 (9)
C1—C2—H2	119.9	C11—C12—C13	120.35 (10)
C13—C14—C15	118.37 (10)	C11—C12—H12	119.8
C13—C14—C17	122.29 (10)	C13—C12—H12	119.8
C15—C14—C17	119.34 (10)	C8—C9—C4	119.86 (10)
C5—C4—C9	118.73 (9)	C8—C9—H9	120.1
C5—C4—C3	116.26 (9)	C4—C9—H9	120.1
C9—C4—C3	125.01 (9)	C9—C8—C7	120.35 (10)
C6—C7—C8	120.80 (10)	C9—C8—H8	119.8
C6—C7—H7	119.6	C7—C8—H8	119.8
C8—C7—H7	119.6	C17—C18—H18A	109.5
C14—C13—C12	120.59 (10)	C17—C18—H18B	109.5
C14—C13—H13	119.7	H18A—C18—H18B	109.5
C12—C13—H13	119.7	C17—C18—H18C	109.5
C7—C6—C5	118.50 (10)	H18A—C18—H18C	109.5
C7—C6—H6	120.7	H18B—C18—H18C	109.5

C10—O3—C3—C2	−110.14 (11)	C8—C7—C6—C5	−0.71 (16)
C10—O3—C3—C4	74.63 (12)	O1—C5—C6—C7	−179.21 (9)
C1—O1—C5—C6	−179.77 (9)	C4—C5—C6—C7	0.81 (16)
C1—O1—C5—C4	0.22 (15)	C13—C14—C17—C18	−8.76 (16)
C3—O3—C10—O4	−0.98 (15)	C15—C14—C17—C18	171.64 (11)
C3—O3—C10—C11	178.33 (8)	C13—C14—C15—C16	−0.28 (17)
C12—C11—C10—O4	−8.15 (17)	C17—C14—C15—C16	179.33 (10)
C16—C11—C10—O4	170.94 (11)	C14—C15—C16—C11	−0.84 (17)
C12—C11—C10—O3	172.57 (9)	C12—C11—C16—C15	1.29 (17)
C16—C11—C10—O3	−8.34 (14)	C10—C11—C16—C15	−177.78 (10)
O3—C3—C2—C1	−175.83 (9)	C5—O1—C1—O2	179.08 (9)
C4—C3—C2—C1	−0.73 (16)	C5—O1—C1—C2	−0.34 (15)
O1—C5—C4—C9	179.49 (9)	C3—C2—C1—O2	−178.76 (11)
C6—C5—C4—C9	−0.53 (16)	C3—C2—C1—O1	0.60 (16)
O1—C5—C4—C3	−0.30 (15)	C16—C11—C12—C13	−0.62 (17)
C6—C5—C4—C3	179.68 (9)	C10—C11—C12—C13	178.49 (10)
C2—C3—C4—C5	0.57 (15)	C14—C13—C12—C11	−0.52 (18)
O3—C3—C4—C5	175.61 (9)	C5—C4—C9—C8	0.14 (16)
C2—C3—C4—C9	−179.20 (10)	C3—C4—C9—C8	179.91 (10)
O3—C3—C4—C9	−4.17 (16)	C4—C9—C8—C7	−0.05 (16)
C15—C14—C13—C12	0.96 (17)	C6—C7—C8—C9	0.34 (17)
C17—C14—C13—C12	−178.64 (11)

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2-Oxo-2H-chromen-4-yl 4-ethylbenzoate . Hydrogen-bond geometry (Å, º)

Cg1 is the centroid of the C1–C5/O1 ring.

D—H···A	D—H	H···A	D···A	D—H···A
C2—H2···O2ⁱ	0.93	2.49	3.4223 (14)	176
C9—H9···O4ⁱⁱ	0.93	2.57	3.4164 (14)	151
C16—H16···O2ⁱⁱⁱ	0.93	2.54	3.4436 (14)	163
C1—O2···Cg1^iv	1.22 (1)	3.27 (1)	3.5408 (14)	93 (1)

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Symmetry codes: (i) −x+3, −y+1, −z; (ii) x−1, y, z; (iii) −x+2, −y+1, −z; (iv) x+1, y, z.

References

Akkol, E. K., Genç, Y., Karpuz, B., Sobarzo-Sánchez, E. & Capasso, R. (2020). Cancers (Basel)12, 1–25. [DOI] [PMC free article] [PubMed]
Farrugia, L. J. (2012). J. Appl. Cryst.45, 849–854.
Gomes, L. R., Low, J. N., Fonseca, A., Matos, M. J. & Borges, F. (2016). Acta Cryst. E72, 926–932. [DOI] [PMC free article] [PubMed]
Koulabiga, Z., Yao, K. H., Abou, A., Djandé, A., Giorgi, M. & Coussan, S. (2024). Am. J. Org. Chem.12, 1–19.
Rigaku OD (2022). CrysAlis PRO. Rigaku Oxford Diffraction, Yarnton, England.
Sheldrick, G. M. (2015a). Acta Cryst. A71, 3–8.
Sheldrick, G. M. (2015b). Acta Cryst. C71, 3–8.
Spek, A. L. (2020). Acta Cryst. E76, 1–11. [DOI] [PMC free article] [PubMed]
Tosun, A., Akkol, E. K. & Yesilada, E. (2009). Z. Naturforsch., C: J. Biosci.64, 56–62. [DOI] [PubMed]
Tuan Anh, H. L., Kim, D.-C., Ko, W., Ha, T. M., Nhiem, N. X., Yen, P. H., Tai, B. H., Truong, L. H., Long, V. N., Gioi, T., Hong Quang, T., Minh, C. V., Oh, H., Kim, Y. C. & Kiem, P. V. (2017). Pharm. Biol.55, 1195–1201. [DOI] [PMC free article] [PubMed]
Westrip, S. P. (2010). J. Appl. Cryst.43, 920–925.
Ziarani, G. M., Moradi, R., Lashgari, N. & Kruger, H. G. (2018). Metal-Free Synthetic Organic Dyes ch. 7, Coumarin dyes pp. 117–125. https://doi.org/10.1016/b978-0-12-815647-6.00007-8.

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Crystal structure: contains datablock(s) I. DOI: 10.1107/S2414314625007345/hb4531sup1.cif

x-10-x250734-sup1.cif^{(1.7MB, cif)}

Structure factors: contains datablock(s) I. DOI: 10.1107/S2414314625007345/hb4531Isup3.hkl

x-10-x250734-Isup3.hkl^{(345KB, hkl)}

x-10-x250734-Isup3.cml^{(5.6KB, cml)}

Supporting information file. DOI: 10.1107/S2414314625007345/hb4531Isup3.cml

CCDC reference: 2481234

Additional supporting information: crystallographic information; 3D view; checkCIF report

[bb1] Akkol, E. K., Genç, Y., Karpuz, B., Sobarzo-Sánchez, E. & Capasso, R. (2020). Cancers (Basel)12, 1–25. [DOI] [PMC free article] [PubMed]

[bb2] Farrugia, L. J. (2012). J. Appl. Cryst.45, 849–854.

[bb3] Gomes, L. R., Low, J. N., Fonseca, A., Matos, M. J. & Borges, F. (2016). Acta Cryst. E72, 926–932. [DOI] [PMC free article] [PubMed]

[bb4] Koulabiga, Z., Yao, K. H., Abou, A., Djandé, A., Giorgi, M. & Coussan, S. (2024). Am. J. Org. Chem.12, 1–19.

[bb5] Rigaku OD (2022). CrysAlis PRO. Rigaku Oxford Diffraction, Yarnton, England.

[bb6] Sheldrick, G. M. (2015a). Acta Cryst. A71, 3–8.

[bb7] Sheldrick, G. M. (2015b). Acta Cryst. C71, 3–8.

[bb8] Spek, A. L. (2020). Acta Cryst. E76, 1–11. [DOI] [PMC free article] [PubMed]

[bb9] Tosun, A., Akkol, E. K. & Yesilada, E. (2009). Z. Naturforsch., C: J. Biosci.64, 56–62. [DOI] [PubMed]

[bb10] Tuan Anh, H. L., Kim, D.-C., Ko, W., Ha, T. M., Nhiem, N. X., Yen, P. H., Tai, B. H., Truong, L. H., Long, V. N., Gioi, T., Hong Quang, T., Minh, C. V., Oh, H., Kim, Y. C. & Kiem, P. V. (2017). Pharm. Biol.55, 1195–1201. [DOI] [PMC free article] [PubMed]

[bb11] Westrip, S. P. (2010). J. Appl. Cryst.43, 920–925.

[bb12] Ziarani, G. M., Moradi, R., Lashgari, N. & Kruger, H. G. (2018). Metal-Free Synthetic Organic Dyes ch. 7, Coumarin dyes pp. 117–125. https://doi.org/10.1016/b978-0-12-815647-6.00007-8.

PERMALINK

2-Oxo-2H-chromen-4-yl 4-ethylbenzoate

Valentin Bationo

Abel Landry Tebily

Akoun Abou

Charles Bavouma Sombié

Rasmané Semdé

Abdoulaye Djandé

Roles

Abstract

Structure description

Figure 1.

Figure 2.