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10082-93-6

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10082-93-6 Usage

General Description

"(9H-PURIN-6-YLAMINO)ACETIC ACID is a chemical compound with the molecular formula C9H9N5O2. It is a derivative of purine and is a member of the class of compounds known as purine nucleobases and analogues. (9H-PURIN-6-YLAMINO)ACETIC ACID is often used in research and pharmaceutical applications as a building block for the synthesis of various biologically active compounds. It has also been studied for its potential therapeutic applications, particularly in the context of anticancer and antiviral treatments. The chemical structure and properties of (9H-PURIN-6-YLAMINO)ACETIC ACID make it a valuable tool for drug discovery and development, as well as for understanding the biochemical processes associated with purine metabolism."

Check Digit Verification of cas no

The CAS Registry Mumber 10082-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,8 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10082-93:
(7*1)+(6*0)+(5*0)+(4*8)+(3*2)+(2*9)+(1*3)=66
66 % 10 = 6
So 10082-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N5O2/c13-4(14)1-8-6-5-7(10-2-9-5)12-3-11-6/h2-3,5H,1H2,(H,13,14)(H,8,9,10,11,12)

10082-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(7H-purin-6-ylamino)acetic acid

1.2 Other means of identification

Product number -
Other names N-9H-purin-6-ylglycine

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:10082-93-6 SDS

10082-93-6Downstream Products

10082-93-6Relevant articles and documents

Synthesis of N6-substituted adenines from 3-methylxanthine

Kochergin,Persanova,Aleksandrova

, p. 455 - 458 (2000)

A series of 6-arylalkyl(hetarylalkyl, cycloalkyl, carboxyalkyl)amino-7-benzyl-2-chloropurines have been synthesized from 3-methylxanthine via the reaction of the intermediate 7-benzyl-2,6-dichloropurine with amines and aminoacids. N6-benzyladenine, N6-(α-furfuryl)adenine (kinetin), and N-(purinyl)glycine have been obtained via the catalytic hydrogenation of 7-benzyl-6-benzyl(furfuryl, carboxymethyl)amino-2-chloropurines.

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Chheda,Hall

, p. 2082,2085 (1966)

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