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23583-46-2

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23583-46-2 Usage

General Description

1-(3-O-acetyl-2-deoxy-5-O-tritylpentofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione is a chemical compound with a complex structure. It contains a pentofuranosyl group, an acetyl group, and a trityl group, as well as a pyrimidine-2,4(1H,3H)-dione moiety. 1-(3-O-acetyl-2-deoxy-5-O-tritylpentofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione is a derivative of thymidine, a nucleoside that is a structural component of DNA. The presence of the acetyl and trityl groups suggests that this compound may be used for chemical synthesis or as a precursor to other compounds. Its specific properties and potential uses would depend on the context in which it is being studied or utilized.

Check Digit Verification of cas no

The CAS Registry Mumber 23583-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,8 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23583-46:
(7*2)+(6*3)+(5*5)+(4*8)+(3*3)+(2*4)+(1*6)=112
112 % 10 = 2
So 23583-46-2 is a valid CAS Registry Number.

23583-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3'-O-acetyl-5'-O-triphenylmethylthymidine

1.2 Other means of identification

Product number -
Other names 3'-O-acetyl-5'-O-trityl-thymidine

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:23583-46-2 SDS

23583-46-2Relevant articles and documents

Exploring the potential of 3′-O-carboxy esters of thymidine as inhibitors of ribonuclease A and angiogenin

Ghosh, Kalyan S.,Debnath, Joy,Dutta, Palash,Sahoo, Bijaya K.,Dasgupta, Swagata

, p. 2819 - 2828 (2008/09/20)

In this study, compounds with a carboxy ester in lieu of the phosphate ester at the 3′-position have been employed to inhibit the ribonucleolytic activity of ribonuclease A (RNase A). Phosphates at the 3′-position of pyrimidine bases are well-known inhibitors of the protein. We have investigated the inhibition of RNase A by 3′-O-carboxy esters of thymidine. The compounds behave as competitive inhibitors with inhibition constants ranging from 42 to 95 μM. The mode of inhibition has also been confirmed by 1H NMR studies of the active site histidines of RNase A. Docking studies have further substantiated the experimental results. The compounds are also found to inhibit the ribonucleolytic activity of angiogenin, a homologous protein and potent inducer of blood vessel formation.

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