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6-(trifluoromethyl)-5H-purine is a chemical compound with the molecular formula C5H3F3N4. It is a derivative of purine, a heterocyclic aromatic organic compound that is a central component of nucleic acids, such as DNA and RNA. The presence of a trifluoromethyl group (-CF3) at the 6-position of the purine ring distinguishes 6-(trifluoromethyl)-5H-purine from other purine derivatives. This modification can significantly alter the chemical and biological properties of the molecule, potentially affecting its reactivity, stability, and interactions with other molecules. 6-(trifluoromethyl)-5H-purine may be of interest in medicinal chemistry and drug development due to its potential to modulate biological processes involving purines, such as enzyme inhibition or activation.

2268-11-3

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2268-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2268-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2268-11:
(6*2)+(5*2)+(4*6)+(3*8)+(2*1)+(1*1)=73
73 % 10 = 3
So 2268-11-3 is a valid CAS Registry Number.

2268-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(trifluoromethyl)-7H-purine

1.2 Other means of identification

Product number -
Other names 6-(TRIFLUOROMETHYL)-9H-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:2268-11-3 SDS

2268-11-3Downstream Products

2268-11-3Relevant 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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