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80817-38-5

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  • 3'-Cytidylic acid,N-benzoyl-2'-deoxy-, 2-chlorophenyl 2-cyanoethyl ester (9CI)

    Cas No: 80817-38-5

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80817-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80817-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,1 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80817-38:
(7*8)+(6*0)+(5*8)+(4*1)+(3*7)+(2*3)+(1*8)=135
135 % 10 = 5
So 80817-38-5 is a valid CAS Registry Number.

80817-38-5SDS

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 N4-benzoyl-2'-deoxycytidine-3'-O-(2-chlorophenyl-2-cyanoethyl)phosphate

1.2 Other means of identification

Product number -
Other names Phosphoric acid (2R,3S,5R)-5-(4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-2-hydroxymethyl-tetrahydro-furan-3-yl ester 2-chloro-phenyl ester 2-cyano-ethyl 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:80817-38-5 SDS

80817-38-5Relevant articles and documents

Synthesis of a gene coding for human lysozyme.

Ikehara,Fujimoto,Aoyama,Yanase,Matsugi,Inaoka,Tokunaga,Uesugi,Iwai,Ohtsuka

, p. 2202 - 2208 (2007/10/02)

-

Simplified Liquid-Phase Preparation of Four Decadeoxyribonucleotides and their Preliminary Spectroscopic Characterization

Denny, William A.,Leupin, Werner,Kearns, David R.

, p. 2372 - 2393 (2007/10/02)

Four self-complementary decadeoxyribonucleotides, dApTpApTpApTpApTpApT,dApTpApTpCpGpApTpApT, dApTpApTpGpCpApTpApT and dApApApApApTpTpTpTpT, were chemically synthesized by the phosphotriester procedure.Efforts were concentrated on keeping the procedure as simple as possible, concomitant with obtaining high-purity products at each step of the process.The decamers were elaborated from the 3'-end, starting with a 3'-O-benzoylated monomer according to the scheme: monomer + monomer -> dimer + dimer -> tetramer + dimer -> hexamer + tetramer -> decamer.Putity of intermediates and of the fully blocked decamers were monitored by chromatography and by 300-MHz 1H-NMR. spectroscopy.The deblocked decadeoxyribonucleotides were characterized by their UV., CD., and 1H-NMR. spectra.

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