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264393

Sigma-Aldrich

2,6-Difluorobenzylamine

97%

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About This Item

Linear Formula:
F2C6H3CH2NH2
CAS Number:
69385-30-4
Molecular Weight:
143.13
EC Number:
273-983-9
MDL number:
MFCD00010144
UNSPSC Code:
12352100
PubChem Substance ID:
24856012
NACRES:
NA.22

Quality Level

100

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

Related Categories

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
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

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

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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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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