263389
3,5-双(三氟甲基)苄胺
technical grade, 80%
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关于此项目
线性分子式:
(CF3)2C6H3CH2NH2
化学文摘社编号:
分子量:
243.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
285-290-9
Beilstein/REAXYS Number:
7209267
MDL number:
Assay:
80%
Form:
solid
产品名称
3,5-双(三氟甲基)苄胺, technical grade, 80%
InChI key
DHVHORCFFOSRBP-UHFFFAOYSA-N
InChI
1S/C9H7F6N/c10-8(11,12)6-1-5(4-16)2-7(3-6)9(13,14)15/h1-3H,4,16H2
SMILES string
NCc1cc(cc(c1)C(F)(F)F)C(F)(F)F
grade
technical grade
assay
80%
form
solid
mp
50-55 °C (lit.)
functional group
amine
fluoro
Quality Level
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Application
3,5-Bis(trifluoromethyl)benzylamine has been used in the preparation of phenyl glycine derivatives.
flash_point_f
172.4 °F - closed cup
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_c
78 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Lihu Yang et al.
Bioorganic & medicinal chemistry letters, 16(14), 3735-3739 (2006-05-16)
Systematic modification of a screening lead yielded a class of potent glycinamide based CCR2 antagonists. The best compound (55, (2S)-N-[3,5-bis(trifluoromethyl)benzyl]-2-{[2-(1-piperidinyl)ethyl]amino}-2-(3-thienyl)acetamide) displayed good binding affinity (IC50=30 and 39 nM) toward human monocytes and CHO cell expressing human CCR2b, respectively. Functionally, it
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