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2-AMINO-4,6-DIFLUOROPYRIMIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

675-11-6

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675-11-6 Usage

Uses

4,6-Difluoropyrimidin-2-amine is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 675-11-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 675-11:
(5*6)+(4*7)+(3*5)+(2*1)+(1*1)=76
76 % 10 = 6
So 675-11-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H3F2N3/c5-2-1-3(6)9-4(7)8-2/h1H,(H2,7,8,9)

675-11-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-difluoropyrimidin-2-amine

1.2 Other means of identification

Product number -
Other names 4,6-difluoro-2-pyrimidinamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:675-11-6 SDS

675-11-6Relevant academic research and scientific papers

2,4,6-Trifluoropyrimidine. Reactions with nitrogen nucleophiles

Delia, Thomas J.,Anderson, Dennis P.,Schomaker, Jennifer M.

, p. 991 - 993 (2007/10/03)

In a continuation of our studies involving the nucleophilic displacement of one of the chlorines from 2,4,6-trichloropyrimidine, we now report the initial displacement of one of the fluorine atoms from 2,4,6-trifluoropyrimidine using both aliphatic and aromatic amines. The monosubstitution products favor 2-substitution with ammonia and ethanolamine while aniline gave the 4-substituted derivative as the preferred product.

MECHANISMS FOR REACTIONS OF HALOGENATED COMPOUNDS. PART 6. INVESTIGATIONS INTO THE ACTIVATING EFFECT OF ORTHO-FLUORINE IN NUCLEOPHILIC AROMATIC SUBSTITUTION

Chambers, Richard D.,Seabury, Mark J.,Williams, D. Lyn H.,Hughes, Nigel

, p. 255 - 258 (2007/10/02)

Separate activating effects for ortho- and meta- fluorine, on nucleophilic aromatic substitution, are determinated for pyrimidine and pyridine systems.Comparisons confirm the importance of ion-dipole interactions for activation by ortho-fluorine.The effects of ortho-fluorine on anionic ?-complexes are also discussed.

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