264393
2,6-二氟苄胺
97%
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关于此项目
线性分子式:
F2C6H3CH2NH2
化学文摘社编号:
分子量:
143.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
273-983-9
MDL number:
产品名称
2,6-二氟苄胺, 97%
InChI key
PQCUDKMMPTXMAL-UHFFFAOYSA-N
InChI
1S/C7H7F2N/c8-6-2-1-3-7(9)5(6)4-10/h1-3H,4,10H2
SMILES string
NCc1c(F)cccc1F
assay
97%
refractive index
n20/D 1.493 (lit.)
density
1.197 g/mL at 25 °C (lit.)
functional group
amine
fluoro
Quality Level
Application
2,6-Difluorobenzylamine has been used in the synthesis of:
- (Z)-N1-(2,6-difluorobenzyl)-N2-(2-amino-1,2-dicyanovinyl)formamidine
- 2,6-difluorobenzyl-guanidine hydrochloride
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
150.8 °F - closed cup
flash_point_c
66 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Facile synthesis of 6-cyano-9-substituted-9 H-purines and their ring expansion to 8-(arylamino)-4-imino-3-methylpyrimidino [5, 4-d] pyrimidines.
Al-Azmi A, et al.
Journal of the Chemical Society. Perkin Transactions 1, 20, 2532-2537 (2001)
K L Min et al.
European journal of biochemistry, 238(2), 446-452 (1996-06-01)
Fourteen new creatine analogues, all with a guanidine function and either a polar or an apolar group instead of the creatine carboxylic function, were tested as potential inhibitors for human creatine kinase by kinetic analysis of their effects on the
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