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. 2018 Oct 19;74(Pt 11):1628–1632. doi: 10.1107/S2056989018014627

Table 2. Experimental details.

Crystal data
Chemical formula C13H8Br2FN3O3
M r 433.04
Crystal system, space group Monoclinic, P21/n
Temperature (K) 296
a, b, c (Å) 16.1360 (14), 4.1745 (3), 21.468 (2)
β (°) 95.026 (7)
V3) 1440.5 (2)
Z 4
Radiation type Mo Kα
μ (mm−1) 5.65
Crystal size (mm) 0.46 × 0.17 × 0.02
 
Data collection
Diffractometer Stoe IPDS 2
Absorption correction Integration (X-RED32; Stoe & Cie, 2002)
T min, T max 0.296, 0.883
No. of measured, independent and observed [I > 2σ(I)] reflections 9546, 2775, 1270
R int 0.113
(sin θ/λ)max−1) 0.617
 
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S 0.051, 0.098, 0.84
No. of reflections 2775
No. of parameters 200
H-atom treatment H-atom parameters constrained
Δρmax, Δρmin (e Å−3) 0.42, −0.28

Computer programs: X-AREA and X-RED (Stoe & Cie, 2002), SHELXT2014 (Sheldrick, 2015a ), SHELXL2017 (Sheldrick, 2015b ), ORTEP-3 for Windows and WinGX (Farrugia, 2012) and PLATON (Spek, 2009).