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19325-92-9

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19325-92-9 Usage

General Description

Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate is a chemical compound that is derived from uridine, a nucleoside that is found in all living forms. The 2'-bromo-2'-deoxy- modification refers to the substitution of a hydrogen atom at the 2' carbon of the deoxyribose sugar with a bromine atom, and the 3',5'-diacetate modification indicates the presence of acetyl groups at the 3' and 5' positions of the uridine molecule. Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate is not naturally occurring and is typically synthesized for research purposes. It may have potential applications in the study of nucleic acids, nucleoside analogs, and biochemical pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 19325-92-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,2 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19325-92:
(7*1)+(6*9)+(5*3)+(4*2)+(3*5)+(2*9)+(1*2)=119
119 % 10 = 9
So 19325-92-9 is a valid CAS Registry Number.

19325-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-di-O-acetyl-2-bromo-2-deoxy-β-D-ribofuranosyl)-uracil

1.2 Other means of identification

Product number -
Other names 3',5'-DIACETYL-2'-BROMO-2'-DEOXYURIDINE

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:19325-92-9 SDS

19325-92-9Relevant articles and documents

Synthesis of 1-(2,3-dideoxy-β-D-glycero-pent-2-enofuranosyl(thymine (d4T; stavudine) from 5-methyluridine

Shiragami,Ineyama,Uchida,Izawa

, p. 47 - 58 (1996)

A practical synthetic method of d4T (3) from 5-methyluridine (2a) was developed. The Marumoto-Mansuri method was modified using 2',3'-O-methoxyethylidene-5-methyluridine (10) as an intermediate to afford 1-(3,5-di-O-acetyl-2-bromo-2-deoxy-β-D-ribofuranosyl)thymine (6a) in high yield with less formation of byproducts. The reaction mechanism was also discussed.

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