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64723-00-8

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64723-00-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64723-00-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,2 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64723-00:
(7*6)+(6*4)+(5*7)+(4*2)+(3*3)+(2*0)+(1*0)=118
118 % 10 = 8
So 64723-00-8 is a valid CAS Registry Number.

64723-00-8SDS

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 [(2R,3S,5R)-2-[[(4-methoxyphenyl)-diphenylmethoxy]methyl]-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-3-yl] benzoate

1.2 Other means of identification

Product number -
Other names Thymidine,5'-O-[(4-methoxyphenyl)diphenylmethyl]-,3'-benzoate

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:64723-00-8 SDS

64723-00-8Relevant articles and documents

Tailoring peptide-nucleotide conjugates (PNCs) for nucleotide delivery in bacterial cells

De, Swarup,Groaz, Elisabetta,Herdewijn, Piet

, p. 2322 - 2348 (2014/04/17)

The design and synthesis of peptide-2′-deoxythymidine-5′-O- monophosphate conjugates as potential active delivery systems for nucleotides into auxotrophic E. coli strains is presented. A series of oligopeptides were allowed to react with 5′-O-(dibenzylphosphate)-2′-deoxythymidine or its suitably 3′-derivatized analogues to give the relevant peptide-nucleotide adducts, by the formation of a biolabile chemical connection. Using strategies based on the principles of orthogonal protection and activation, rational variations were made to the linker and the peptide moiety in order to tune the metabolic stability of the conjugates.

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