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107036-56-6

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107036-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107036-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,3 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107036-56:
(8*1)+(7*0)+(6*7)+(5*0)+(4*3)+(3*6)+(2*5)+(1*6)=96
96 % 10 = 6
So 107036-56-6 is a valid CAS Registry Number.

107036-56-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2',3'-dideoxy-5-methylcytidine

1.2 Other means of identification

Product number -
Other names 5-methyl-2',3'-dideoxycytidine

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:107036-56-6 SDS

107036-56-6Downstream Products

107036-56-6Relevant articles and documents

Improved synthesis of 2',3'-dideoxycytidine (d2C) and its correlated nucleoside analogues

De Napoli,Messere,Montesarchio,Piccialli,Santacroce

, p. 981 - 992 (1993)

2',3'-deoxy and 2',3'-dideoxy-2',3'-didehydrocytidine (d2C and d4C) have been synthesized in good yields from 2'-deoxyuridine via dichlorinated derivatives 7a-b. The same synthetic strategy was used in the synthesis of d2C(Me) and d4C(Me) from thymidine. Following this method the evaluable 3'-chloro-2'-deoxycytidine derivatives 9-12 can be easily obtained.

Potent Anti-AIDS Drugs. 2',3'-Dideoxycytidine Analogues

Kim, Chong-Ho,Marquez, Victor E.,Broder, Samuel,Mitsuya, Hiroaki,Driscoll, John S.

, p. 862 - 866 (2007/10/02)

5-Substituted 2',3'-dideoxycytidine analogues have been synthesized and evaluated in vitro for their capabilities to protect T4+ lymphocytes from the cytopathic effects of the HTLV-III/LAV (HIV) virus, the causative agent of acquired immunodefi

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