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264393

Sigma-Aldrich

2,6-Difluorobenzylamine

97%

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1 G
¥5,630
5 G
¥8,370

¥5,630

Available to ship onApril 10, 2025Details

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1 G
¥5,630
5 G
¥8,370

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

¥5,630

Available to ship onApril 10, 2025Details

Request a Bulk Order

Assay

97%

refractive index

n20/D 1.493 (lit.)

density

1.197 g/mL at 25 °C (lit.)

functional group

amine
fluoro

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[1]
  • 2,6-difluorobenzyl-guanidine hydrochloride[2]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

264393-5G:
264393-1G:
264393-BULK:
264393-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM5738
BCCK4373
BCCD6710
BCBZ7454
BCBV8952

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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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