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
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
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)
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