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Merck
CN

264393

2,6-Difluorobenzylamine

97%

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About This Item

Linear Formula:
F2C6H3CH2NH2
CAS Number:
Molecular Weight:
143.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
273-983-9
MDL number:
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Product Name

2,6-Difluorobenzylamine, 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

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

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


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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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