290319
3,5-二氟苄基溴
98%
别名:
α-溴-3,5-二氟甲苯
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关于此项目
线性分子式:
F2C6H3CH2Br
化学文摘社编号:
分子量:
207.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
3,5-二氟苄基溴, 98%
InChI
1S/C7H5BrF2/c8-4-5-1-6(9)3-7(10)2-5/h1-3H,4H2
SMILES string
Fc1cc(F)cc(CBr)c1
InChI key
KVSVNRFSKRFPIL-UHFFFAOYSA-N
assay
98%
refractive index
n20/D 1.521 (lit.)
bp
65 °C/4.5 mmHg (lit.)
density
1.6 g/mL at 25 °C (lit.)
functional group
bromo
fluoro
Quality Level
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
179.6 °F - closed cup
flash_point_c
82 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
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Highly efficient N-heterocyclic carbene/pyridine-based ruthenium sensitizers: complexes for dye-sensitized solar cells.
Wei-Chun Chang et al.
Angewandte Chemie (International ed. in English), 49(44), 8161-8164 (2010-09-22)
Ya-Tuan Ma et al.
Acta crystallographica. Section E, Structure reports online, 66(Pt 9), o2468-o2468 (2010-01-01)
The title compound, C(15)H(12)F(2)O(3), has been obtained by the reaction of 2,4-dihy-droxy-lacetonephenone, potassium carbonate and 3,5-difluoro-benzyl bromide. The hy-droxy group is involved in an intra-molecular O-H⋯O hydrogen bond in each of the two independent mol-ecules in the asymmetric unit. The
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