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2-Bromo-2-deoxy-5-methyluridine-3,5-diacetate is a nucleoside derivative belonging to the class of nucleosides, which are the building blocks of nucleic acids like DNA and RNA. It is a modified form of uridine, a naturally occurring nucleoside, with the addition of a bromine atom, a methyl group, and two acetate groups. These modifications can potentially influence the compound's solubility, stability, and biological activity.

95585-76-5

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95585-76-5 Usage

Uses

Used in Medicinal Chemistry:
2-Bromo-2-deoxy-5-methyluridine-3,5-diacetate is used as a chemical intermediate for the synthesis of nucleoside analogs, which can be further developed into potential therapeutic agents. Its unique structure allows for the exploration of its interactions with biological targets and the development of new drugs.
Used in Biochemistry:
In biochemistry, 2-Bromo-2-deoxy-5-methyluridine-3,5-diacetate can be utilized as a research tool to study the mechanisms of nucleic acid synthesis and function. Its modified structure can provide insights into the role of specific functional groups in nucleoside recognition and binding.
Used in Pharmaceutical Research:
2-Bromo-2-deoxy-5-methyluridine-3,5-diacetate is used as a starting material in the development of novel nucleoside analogs for therapeutic purposes. Its potential applications in medicinal chemistry and biochemistry make it a valuable compound for the design and synthesis of new pharmaceuticals.
Used in the Development of Nucleoside Analogs:
2-Bromo-2-deoxy-5-methyluridine-3,5-diacetate is used as a precursor in the synthesis of nucleoside analogs that can be employed as antiviral, anticancer, or immunosuppressive agents. Its unique structural features can contribute to the development of more effective and targeted therapies.
Further studies and investigations are necessary to fully understand the chemical and biological properties of 2-Bromo-2-deoxy-5-methyluridine-3,5-diacetate and its potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 95585-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95585-76:
(7*9)+(6*5)+(5*5)+(4*8)+(3*5)+(2*7)+(1*6)=185
185 % 10 = 5
So 95585-76-5 is a valid CAS Registry Number.

95585-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2'-Bromo-2'-deoxy-3,4-dihydrothymidine

1.2 Other means of identification

Product number -
Other names 2-Brom-thiophen-3-carboxamid

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:95585-76-5 SDS

95585-76-5Relevant academic research and scientific papers

Method for preparing β-thymidine

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Paragraph 0099-0101, (2018/02/04)

The invention relates to a preparation method of beta-thymidine, and specifically discloses a method of preparing beta-thymidine from the formula II compound. The method comprises following steps: subjecting the compound represented as the formula II to carry out dehalogenation reactions, in a hydrogen atmosphere, in the presence of a catalyst, and in a buffer system with a pH value of 6.5 to 8.0, so as to obtain beta-thymidine represented as the formula I, wherein X represents Cl or Br. The dehalogenation reactions are carried out under atmospheric pressure, and the preparation method has the advantages of environment-friendliness, economy, high product yield, good product purity, and suitability for industrial production.

Discovery of a Novel Route to β-Thymidine: a Precursor for anti-AIDS Compounds

Rao, A. V. Rama,Gurjar, Mukund K.,Lalitha, Sista V. S.

, p. 1255 - 1256 (2007/10/02)

A new approach to the synthesis of β-thymidine from D-xylose is described.

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