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5173-91-1

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5173-91-1 Usage

General Description

Uridine, 2'-deoxy-, 3',5'-bis(4-chlorobenzoate) is a chemical compound that consists of a molecule of uridine, which is a nucleoside that plays a role in the synthesis of RNA, and two molecules of 4-chlorobenzoate. Uridine, 2'-deoxy-, 3',5'-bis(4-chlorobenzoate) is used in biochemical research as a substrate for enzymes involved in nucleotide metabolism. It can also be used as a precursor for the synthesis of other nucleotide analogs, which have potential applications in medicinal chemistry and drug development. Uridine, 2'-deoxy-, 3',5'-bis(4-chlorobenzoate) is an important tool for studying the mechanisms of nucleotide synthesis and metabolism in living organisms.

Check Digit Verification of cas no

The CAS Registry Mumber 5173-91-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5173-91:
(6*5)+(5*1)+(4*7)+(3*3)+(2*9)+(1*1)=91
91 % 10 = 1
So 5173-91-1 is a valid CAS Registry Number.

5173-91-1SDS

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 ((2R,3S,5R)-3-((4-chlorobenzoyl)oxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl 4-chlorobenzoate

1.2 Other means of identification

Product number -
Other names -

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:5173-91-1 SDS

5173-91-1Relevant articles and documents

An efficient amination method for manufacturing cytidines

Komatsu, Hironori,Morizane, Kunihiko,Kohno, Toshiyuki,Tanikawa, Hiroharu

, p. 564 - 567 (2013/09/02)

A novel method for amination of uridine derivatives was developed and applied to the syntheses of cytidines. The method consists of an activation step with 1-methylpiperidine at the C4-position of a uracil base. Large-scale preparation of 2′-deoxycytidine was performed using this method.

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