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90794-98-2

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90794-98-2 Usage

Chemical compound

6-chloro-9-(5-methyltetrahydrofuran-2-yl)-9H-purine

Class of compound

purine

Main properties

Chlorine atom at the 6 position
5-methyltetrahydrofuran-2-yl group attached to the 9 position

Potential applications

Pharmaceutical and drug development
Antiviral and anticancer drugs
Research tool in biochemistry and molecular biology

Specific content

Modified form of the nucleobase purine
Used to study the structure and function of nucleic acids and related biomolecules

Check Digit Verification of cas no

The CAS Registry Mumber 90794-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,9 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90794-98:
(7*9)+(6*0)+(5*7)+(4*9)+(3*4)+(2*9)+(1*8)=172
172 % 10 = 2
So 90794-98-2 is a valid CAS Registry Number.

90794-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-9-(5-methyloxolan-2-yl)purine

1.2 Other means of identification

Product number -
Other names BG 100

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:90794-98-2 SDS

90794-98-2Downstream Products

90794-98-2Relevant articles and documents

Simple and convenient synthesis method of N9-alkylate nucleoside analogs on purine framework

-

Paragraph 0075; 0076; 0077; 0078; 0079; 0080, (2018/03/26)

The invention discloses a simple and convenient synthesis method of N9-alkylate nucleoside analogs on a purine framework. The method comprises the following steps that 2,6-site substituted purine derivatives and excessive alkyl ether are added into a reactor; next, non-metallic catalysts and oxidizing agents are added; oxidization coupling reaction is performed under the heating and stirring conditions; thin layer chromatography is used for tracking the reaction; after the reaction is completed, the materials are cooled to the room temperature; vacuum concentration is performed to remove solvents; column chromatography purification is performed; the N9-alkylate nucleoside analogs on the purine framework are obtained. The synthesis method provided by the invention has the advantages that the raw materials are cheap and can be easily obtained; the reaction conditions are mild; the reaction steps are few; the operation is simple; the problems of easy poisoning by metal catalysts, compatibility difficulty of active groups and many reaction sites in the purine derivatization reaction in the prior art are solved; the N9-alkylate nucleoside analogs on the purine framework can be efficiently synthesized.

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