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Cyclopentanecarboxylic acid, 1-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-oxo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

744217-31-0

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744217-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 744217-31-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,4,2,1 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 744217-31:
(8*7)+(7*4)+(6*4)+(5*2)+(4*1)+(3*7)+(2*3)+(1*1)=150
150 % 10 = 0
So 744217-31-0 is a valid CAS Registry Number.

744217-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(tert-butyldiphenylsilyloxymethyl)-2-oxo-cyclopentanecarboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 1-(tert-Butyl-diphenyl-silanyloxymethyl)-2-oxo-cyclopentanecarboxylic acid methyl ester

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:744217-31-0 SDS

744217-31-0Relevant academic research and scientific papers

Anti-viral nucleoside analogs and methods for treating viral infections, especially HIV infections

-

Page/Page column 26, (2015/09/28)

The present invention relates to novel compounds according to the general formulas I, II, III, IV or V: wherein B is nucleoside base according to the structure: and the remaining variables as defined in the specification, and pharmaceutical compositions c

Synthesis of (±)-4′-ethynyl and 4′-cyano carbocyclic analogues of stavudine (d4T)

Kumamoto, Hiroki,Haraguchi, Kazuhiro,Tanaka, Hiromichi,Nitanda, Takao,Baba, Masanori,Dutschman, Ginger E.,Cheng, Yung-Chi,Kato, Keisuke

, p. 73 - 83 (2007/10/03)

The synthesis of (±)-4′-ethynyl (8) and 4′-cyano (9) carbocyclic analogues of the anti-HIV agent stavudine (5, d4T) is reported. The carbocyclic unit (16) was constructed from readily available β-keto ester 10. The ethynyl or cyano group of 8 and 9 were p

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