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Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate is a synthetic chemical compound derived from uridine, a nucleoside present in all living organisms. Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate features a bromine atom at the 2' position of the deoxyribose sugar, replacing a hydrogen atom, and acetyl groups at the 3' and 5' positions of the uridine molecule. It is not naturally occurring and is primarily synthesized for research purposes, with potential applications in the study of nucleic acids, nucleoside analogs, and biochemical pathways.

19325-92-9

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19325-92-9 Usage

Uses

Used in Research Applications:
Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate is used as a research tool for investigating the structure and function of nucleic acids and their interactions with proteins and other molecules. The unique modifications in Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate allow researchers to explore its effects on various biochemical processes and pathways.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate may be utilized as a starting material or intermediate in the synthesis of novel nucleoside analogs with potential therapeutic applications. These analogs could be developed as antiviral, anticancer, or antimicrobial agents, depending on their specific properties and interactions with biological targets.
Used in Biochemical Pathway Studies:
Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate can be employed in the study of biochemical pathways involving nucleosides and nucleotides, such as those involved in DNA replication, RNA synthesis, and cellular energy metabolism. Understanding the role of Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate in these pathways can provide insights into the development of new therapeutic strategies for various diseases.
Used in Diagnostic Applications:
Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate may also find use in diagnostic applications, such as the development of assays or sensors for detecting specific enzymes or proteins involved in nucleic acid metabolism. The unique structural features of Uridine, 2'-bromo-2'-deoxy-, 3',5'-diacetate can be exploited to design highly specific and sensitive diagnostic tools.

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 academic research and scientific papers

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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