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2-amino-1-methyl-9-pentofuranosyl-7,9-dihydro-1H-purine-6,8-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27964-07-4

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27964-07-4 Usage

General Description

2-amino-1-methyl-9-pentofuranosyl-7,9-dihydro-1H-purine-6,8-dione is an organic compound that belongs to the family of purines. It is a derivative of the nucleoside adenosine and is an important component of DNA and RNA. This chemical is commonly known as Adenine, one of the four nucleobases that make up the genetic code in DNA and RNA. Adenine plays a crucial role in storing and transferring genetic information in living organisms. It is also involved in various biological processes, such as energy metabolism and signal transduction. Furthermore, Adenine is an essential component of many coenzymes, such as NAD and FAD, which are involved in various metabolic pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 27964-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,6 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27964-07:
(7*2)+(6*7)+(5*9)+(4*6)+(3*4)+(2*0)+(1*7)=144
144 % 10 = 4
So 27964-07-4 is a valid CAS Registry Number.

27964-07-4SDS

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 2-amino-9-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1-methyl-7H-purine-6,8-dione

1.2 Other means of identification

Product number -
Other names 1-methyl-8-hydroxyguanosine

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:27964-07-4 SDS

27964-07-4Upstream product

27964-07-4Downstream Products

27964-07-4Relevant academic research and scientific papers

ELECTROPHILIC AMINATION OF GUANINE DERIVATIVES. MECHANISM FOR FORMATION OF 8-AMINOGUANINE DERIVATIVES

Kohda, Kohfuku,Baba, Kunihisa,Kawazoe, Yutaka

, p. 1531 - 1540 (2007/10/02)

A study of the mechanism of 8-aminoguanosine formation in the reaction of guanosine with hydroxylamine-O-sulfonic acid (HAOS) revealed that the reaction proceeds in three steps; 1) electrophilic N-7 amination by HAOS, 2) nucleophilic C-8 hydroxyamination by NH2OH accompanied by elimination of the N-7 amino group and by aromatization, and finally 3) the reduction of the C-8 hydroxyamino group by NH2OH to give 8-aminoguanosine.The significance of formation of the 7-aminoguanosine intermediate is discussed briefly in relation to thr reaction of carcinogenic arylamines and arylhydroxylamines with cellular DNA.

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