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Thymidine, 2',3'-didehydro-3'-deoxy-, 5'-(phenylmethyl phosphonate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

244642-02-2

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244642-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 244642-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,6,4 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 244642-02:
(8*2)+(7*4)+(6*4)+(5*6)+(4*4)+(3*2)+(2*0)+(1*2)=122
122 % 10 = 2
So 244642-02-2 is a valid CAS Registry Number.

244642-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name O-benzyl-O'-(2',3'-didehydro-2',3'-dideoxythymidin-5'-yl) phosphonate

1.2 Other means of identification

Product number -
Other names benzyl 2',3'-didehydro-2',3'-dideoxythymidin-5-yl H-phosphonate

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:244642-02-2 SDS

244642-02-2Downstream Products

244642-02-2Relevant academic research and scientific papers

Novel benzyl rearrangements in electrospray ionization multistage tandem mass spectra of benzyl 2',3'- didehydro-2',3'-dideoxythymidin-5'-yl H-phosphonate.

Chen,Sun, Xiaobin,Fu, Hua,Liu, Xiaohong,Zhao, Yufen

, p. 730 - 735 (2004)

Several alkyl 2',3'-didehydro-2',3'-dideoxythymidin-5'-yl H-phosphonates were synthesized and analyzed by electrospray ionization multistage tandem mass spectrometry (ESI-MS(n)). Two kinds of novel benzyl rearrangement reactions were observed in ESI - MS(

Synthesis of AZT/d4T boranophosphates as anti-HIV prodrug candidates

Lin, Changxue,Fu, Hua,Tu, Guangzhong,Zhao, Yufen

, p. 509 - 516 (2007/10/03)

AZT/d4T phosphonates were synthesized by sequential condensation of AZT/ d4T with the corresponding alcohols or 5′-DMT-thymidine in the presence of pivaloyl chloride. Sequential silylation, boronation, and hydrolysis in ammonium hydroxide of these phosphonates led to anti-HIV prodrug candidates AZT/d4T boranophosphates.

One-pot synthesis of hydrogen phosphonate derivatives of d4T and AZT.

Sun, Xiao Bin,Kang, Jian Xun,Zhao, Yu Fen

, p. 2414 - 2415 (2007/10/03)

A simple and one-pot route for the synthesis of d4T or AZT hydrogen phosphonate derivatives via reaction of d4T or AZT with phosphorus trichloride, then alcoholysis and dealkylation in the presence of the corresponding alcohol is described.

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