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17405-22-0

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17405-22-0 Usage

Structure

Six-membered nitrogen-containing ring with a hydroxyl group attached to the sixth carbon atom

Derivative

Purine base, commonly found in nucleic acids such as DNA and RNA

Biochemical processes

Involved in various processes in living organisms, plays a crucial role in the synthesis of nucleotides and nucleic acids

Pharmaceutical applications

Potential anti-inflammatory and immunomodulatory properties, currently being studied.

Check Digit Verification of cas no

The CAS Registry Mumber 17405-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,0 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17405-22:
(7*1)+(6*7)+(5*4)+(4*0)+(3*5)+(2*2)+(1*2)=90
90 % 10 = 0
So 17405-22-0 is a valid CAS Registry Number.

17405-22-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7H-purin-6-ylmethanol

1.2 Other means of identification

Product number -
Other names 6-Hydroxy-methyl-purin

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:17405-22-0 SDS

17405-22-0Downstream Products

17405-22-0Relevant articles and documents

Synthesis of 2-substituted 6-(hydroxymethyl)purine bases and nucleosides

Silhar, Peter,Pohl, Radek,Votruba, Ivan,Hocek, Michal

, p. 1669 - 1695 (2007/10/03)

A facile and efficient methodology of the synthesis of 6-(hydroxymethyl) purine derivatives (bases and nucleosides) was developed based on Pd-catalyzed cross-coupling reactions of 6-halopurines or N-protected 2-amino-6-halopurines with (benzoyloxymethyl)z

Preparation and properties of a 6- and 2.6-substituted purine

Giner-Sorolla

, p. 611 - 618 (2007/10/05)

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