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[6-amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydrofuran-2-yl)-9H-purin-8-ylamino]-acetic acid is a complex organic compound with a molecular formula of C15H19N7O6. It is a derivative of purine, a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. This specific compound features a 6-amino group attached to the purine ring, and a 9-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydrofuran-2-yl)-9H-purin-8-ylamino group connected to the acetic acid moiety. The compound's structure is characterized by the presence of multiple chiral centers, which contribute to its stereochemistry. It is a white crystalline solid and is soluble in water. [6-amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydrofuran-2-yl)-9H-purin-8-ylamino]-acetic acid is of interest in the field of medicinal chemistry, particularly in the development of potential therapeutic agents targeting purine-related metabolic pathways.

87650-99-5

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87650-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87650-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,5 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87650-99:
(7*8)+(6*7)+(5*6)+(4*5)+(3*0)+(2*9)+(1*9)=175
175 % 10 = 5
So 87650-99-5 is a valid CAS Registry Number.

87650-99-5SDS

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 [6-amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydrofuran-2-yl)-9H-purin-8-ylamino]-acetic acid

1.2 Other means of identification

Product number -
Other names N-(adenosin-8-yl)glycine

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:87650-99-5 SDS

87650-99-5Downstream Products

87650-99-5Relevant academic research and scientific papers

A NEW METHOD FOR THE PREPARATION OF N-(NUCLEOSIDYL)-α-AMINO ACIDS USING TRIOCTYLMETHYLAMMONIUM SALTS OF α-AMINO ACIDS

Schroeder, Frank Roland,Cramer, Friedrich

, p. 3571 - 3572 (1983)

8-Bromoadenosine reacts with trioctylmethylammonium salts of α-amino acids (e.g. glycine) to yield N-(adenosin-8-yl)-α-amino acids which can be readily separated from the starting material by two subsequent extraction steps at different pH values.

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