所有图片(1)
About This Item
线性分子式:
CF3C6H4B(OH)2
CAS号:
分子量:
189.93
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
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方案
≥95.0%
表单
solid
mp
111-114 °C (lit.)
官能团
fluoro
SMILES字符串
OB(O)c1ccccc1C(F)(F)F
InChI
1S/C7H6BF3O2/c9-7(10,11)5-3-1-2-4-6(5)8(12)13/h1-4,12-13H
InChI key
JNSBEPKGFVENFS-UHFFFAOYSA-N
应用
2-(Trifluoromethyl)phenylboronic acid can be used as a reactant:
- In Suzuki-coupling reactions to prepare 2-trifluoromethyl aryl or heteroaryl derivatives.
- To synthesize 4-(2-trifluoromethyl)phenylpyrrolo[2,3-d]pyrimidine as a potential antagonist of corticotropin-releasing hormone.
- To prepare 2-nitro-6-(trifluoromethyl)phenylboronic acid by nitration reaction.
其他说明
含不定量的酸酐
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
Studies of palladium-catalyzed coupling reactions for preparation of hindered 3-arylpyrroles relevant to (-)-rhazinilam and its analogues
Ghosez L, et al.
Canadian Journal of Chemistry, 79(11), 1827-1839 (2001)
Efficient synthetic approach to heterocycles possessing the 3, 3-disubstituted-2, 3-dihydrobenzofuran skeleton via diverse palladium-catalyzed tandem reactions
Szlosek-Pinaud M, et al.
Tetrahedron, 63(16), 3340-3349 (2007)
Functionalization of pyrrolo [2, 3-d] pyrimidine by palladium-catalyzed cross-coupling reactions
Tumkevicius, S and Dodonova, J
Chemistry of Heterocyclic Compounds, 48(2), 258-279 (2012)
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