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. 2026 Sep 3;11(Pt 9):x260892. doi: 10.1107/S2414314626008928

Table 2. Experimental details.

Crystal data
Chemical formula C15H10Cl2N2
M r 289.15
Crystal system, space group Orthorhombic, Aea2
Temperature (K) 150
a, b, c (Å) 13.7569 (4), 26.2508 (8), 7.1470 (2)
V (Å3) 2580.99 (13)
Z 8
Radiation type Cu Kα
μ (mm−1) 4.40
Crystal size (mm) 0.21 × 0.11 × 0.06
 
Data collection
Diffractometer Bruker AXS D8 Quest
Absorption correction Multi-scan (SADABS; Krause et al., 2015 ▸)
Tmin, Tmax 0.500, 0.754
No. of measured, independent and observed [I > 2σ(I)] reflections 35150, 2788, 2646
R int 0.064
(sin θ/λ)max (Å−1) 0.640
 
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.029, 0.078, 1.11
No. of reflections 2788
No. of parameters 173
No. of restraints 1
H-atom treatment H-atom parameters constrained
Δρmax, Δρmin (e Å−3) 0.23, −0.28
Absolute structure Flack x determined using 1146 quotients [(I+)−(I−)]/[(I+)+(I−)] (Parsons et al., 2013 ▸)
Absolute structure parameter 0.004 (7)

Computer programs: APEX6 and SAINT (Bruker, 2026 ▸), SHELXT (Sheldrick, 2015a ▸), SHELXL2025/1 (Sheldrick, 2015b ▸), OLEX2 (Dolomanov et al., 2009 ▸), ORTEP-3 for Windows (Farrugia, 2012 ▸) and Mercury (Macrae et al., 2020 ▸).