2,6-Difluorobenzylamine

Suppliers

Names

[ Name ]:
2,6-Difluorobenzylamine

[Synonym ]:
1-(2,6-Difluorophenyl)methylamine
EINECS 273-983-9
Z1R BF FF
(2,6-Difluorophenyl)methylamine
2,6-Difluorobenzenemethanamine
1-(2,6-Difluorophenyl)methanamine
2,6-Difluorobenzylamine
(2,6-Difluorophenyl)methanamine
Benzenemethanamine, 2,6-difluoro-
MFCD00010144

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
172.6±25.0 °C at 760 mmHg

[ Molecular Formula ]:
C₇H₇F₂N

[ Molecular Weight ]:
143.134

[ Flash Point ]:
65.6±0.0 °C

[ Exact Mass ]:
143.054657

[ PSA ]:
26.02000

[ LogP ]:
1.23

[ Vapour Pressure ]:
1.3±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.501

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S27-S36/37/39-S45-S25

[ RIDADR ]:
UN 2735 8/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
29214980

Precursor & DownStream

Precursor

2,6-Difluorobenzyl chloride
2,6-difluorobenzaldehyde oxime

DownStream

N-[(2,6-difluorophenyl)methyl]-3-nitropyridin-4-amine
5-BROMO-1-(2,6-DIFLUORO-BENZYL)-6-METHYL-1H-PYRIMIDINE-2,4-DIONE
1-(2,6-DIFLUORO-BENZYL)-6-METHYL-1H-PYRIMIDINE-2,4-DIONE
(2,6-Difluoro-benzyl)-urea

Customs

[ HS Code ]: 2921499090

[ Summary ]:
2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Synthesis and differential properties of creatine analogues as inhibitors for human creatine kinase isoenzymes.

Eur. J. Biochem. 238(2) , 446-52, (1996)

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...

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.

J. Chem. Soc. Perkin Trans. I 20 , 2532-37, (2001)

2,6-difluorobenzylamine
3-Ethoxy-2,6-difluorobenzylamine
3-chloro-2,6-difluorobenzylamine
3-CHLORO-2,6-DIFLUOROBENZYLAMINE
(2,6-Dichlorobenzyl)methylamine hydrochloride
2,6-Dimethylimidazo[1,2-a]pyridine-3-carbaldehyde
3-(2-Oxo-1,2,3,4-tetrahydroquinolin-6-yl)benzonitrile
3-{[3-oxo-6-(piperidine-1-sulfonyl)-2H,3H-[1,2,4]triazolo[4,3-a]pyridin-2-yl]methyl}benzonitrile
2-[(2-fluorophenyl)methyl]-6-(piperidine-1-sulfonyl)-2H,3H-[1,2,4]triazolo[4,3-a]pyridin-3-one
2-[(3-fluorophenyl)methyl]-6-(piperidine-1-sulfonyl)-2H,3H-[1,2,4]triazolo[4,3-a]pyridin-3-one
2-[(4-fluorophenyl)methyl]-6-(piperidine-1-sulfonyl)-2H,3H-[1,2,4]triazolo[4,3-a]pyridin-3-one
2-[(3,5-difluorophenyl)methyl]-6-(piperidine-1-sulfonyl)-2H,3H-[1,2,4]triazolo[4,3-a]pyridin-3-one
2-(3-chlorobenzyl)-6-(piperidin-1-ylsulfonyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one
2-(4-chlorobenzyl)-6-(piperidin-1-ylsulfonyl)[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one
6-(piperidine-1-sulfonyl)-2-{[3-(trifluoromethyl)phenyl]methyl}-2H,3H-[1,2,4]triazolo[4,3-a]pyridin-3-one
2-methyl-6-((4-methylpiperidin-1-yl)sulfonyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one

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