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6-(trifluoromethyl)-5H-purin-2-amine, also known as 6-trifluoromethylpurine-2-amine, is a chemical compound with the molecular formula C6H4F3N5. It is a derivative of purine, a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. The presence of a trifluoromethyl group at the 6-position and an amino group at the 2-position distinguishes 6-(trifluoromethyl)-5H-purin-2-amine from other purine derivatives. This specific structure may confer unique chemical and biological properties, making it potentially useful in the development of pharmaceuticals or as a research tool in the study of purine-based compounds.

2993-20-6

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2993-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2993-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2993-20:
(6*2)+(5*9)+(4*9)+(3*3)+(2*2)+(1*0)=106
106 % 10 = 6
So 2993-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H4F3N5/c7-6(8,9)3-2-4(12-1-11-2)14-5(10)13-3/h1-2H,(H2,10,11,12,14)

2993-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(trifluoromethyl)-5H-purin-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-6-(trifluoromethyl)purine

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:2993-20-6 SDS

2993-20-6Downstream Products

2993-20-6Relevant academic research and scientific papers

Perfluoroalkylation of 6-iodopurines by trimethyl(perfluoroalkyl)silanes. Synthesis of 6-(perfluoroalkyl)purine bases, nucleosides and acyclic nucleotide analogues

Hocek, Michal,Holy, Antonin

, p. 229 - 241 (2007/10/03)

A Cul/KF mediated perfluoroalkylation reaction of various 9-substituted 6-iodopurines 1 with trimethyl(trifluoromethyl)silane or heptafluoropropyl(trimethyl)silane was used for the synthesis of the corresponding 6-(trifluoromethyl)-and 6-(heptafluoropropy

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