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About This Item
Linear Formula:
F2C6H3CH2NH2
CAS Number:
Molecular Weight:
143.13
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
refractive index
n20/D 1.493 (lit.)
density
1.197 g/mL at 25 °C (lit.)
SMILES string
NCc1c(F)cccc1F
InChI
1S/C7H7F2N/c8-6-2-1-3-7(9)5(6)4-10/h1-3H,4,10H2
InChI key
PQCUDKMMPTXMAL-UHFFFAOYSA-N
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
150.8 °F - closed cup
Flash Point(C)
66 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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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