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[5-(6-aminopurin-9-yl)-4-[[5-(6-aminopurin-9-yl)-4-hydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl]oxy-3-hydroxy-tetrahydrofuran-2-yl]methyl [2-(6-aminopurin-9-yl)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-3-yl] hydrogen phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77244-91-8

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77244-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77244-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,4 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77244-91:
(7*7)+(6*7)+(5*2)+(4*4)+(3*4)+(2*9)+(1*1)=148
148 % 10 = 8
So 77244-91-8 is a valid CAS Registry Number.

77244-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(6-aminopurin-9-yl)-5-[[[2-(6-aminopurin-9-yl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl]oxy-hydroxyphosphoryl]oxymethyl]-4-hydroxyoxolan-3-yl] [5-(6-aminopurin-9-yl)-4-hydroxyoxolan-2-yl]methyl hydrogen phosphate

1.2 Other means of identification

Product number -
Other names Adenosine,adenosine,cordycepin

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:77244-91-8 SDS

77244-91-8Upstream product

77244-91-8Downstream Products

77244-91-8Relevant academic research and scientific papers

Synthesis of 2′-end modified 2′-5′-adenylate trimers

Engels, Joachim

, p. 4339 - 4342 (2007/10/02)

Trimeric 2′,5′-linked adenylates incorporating deoxyribosides and arabinoside of adenine in the 2′-end were synthesized by the phosphotriester approach using quinoline-8-sulfonyl nitrotriazoline as an effective condensing agent.

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