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155-11-3

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155-11-3 Usage

Description

2,4-Pyrimidinediamine, 5-fluoro(9CI) is a pyrimidine derivative that is fluorinated at the 5-position. It is a chemical compound with potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. 2,4-Pyrimidinediamine, 5-fluoro(9CI) is known for its potential as an antitumor and antiviral agent, as well as its possible use as an anti-inflammatory and immunosuppressive agent. However, further research is needed to fully understand its biological activities and potential toxicity for safe and effective pharmaceutical use.

Uses

Used in Pharmaceutical Industry:
2,4-Pyrimidinediamine, 5-fluoro(9CI) is used as a building block for the synthesis of various drugs due to its potential antitumor and antiviral properties.
Used in Antitumor Applications:
2,4-Pyrimidinediamine, 5-fluoro(9CI) is used as an antitumor agent, with potential applications in the development of drugs targeting cancer cells.
Used in Antiviral Applications:
2,4-Pyrimidinediamine, 5-fluoro(9CI) is used as an antiviral agent, with potential applications in the development of drugs targeting viral infections.
Used in Anti-inflammatory Applications:
2,4-Pyrimidinediamine, 5-fluoro(9CI) is used as an anti-inflammatory agent, with potential applications in the development of drugs targeting inflammation-related conditions.
Used in Immunosuppressive Applications:
2,4-Pyrimidinediamine, 5-fluoro(9CI) is used as an immunosuppressive agent, with potential applications in the development of drugs targeting autoimmune diseases and transplant rejection.

Check Digit Verification of cas no

The CAS Registry Mumber 155-11-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155-11:
(5*1)+(4*5)+(3*5)+(2*1)+(1*1)=43
43 % 10 = 3
So 155-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H5FN4/c5-2-1-8-4(7)9-3(2)6/h1H,(H4,6,7,8,9)

155-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-fluoropyrimidine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 2,4-Pyrimidinediamine,5-fluoro

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:155-11-3 SDS

155-11-3Downstream Products

155-11-3Relevant articles and documents

Synthesis of 5-Fluorocytosine Using 2-Cyano-2-fluoroethenolate as a Key Intermediate

Dietz, Jule-Philipp,Derstine, Brenden P.,Ferenc, Dorota,Crawford, Evan T.,Arduengo, Anthony J.,Gupton, B. Frank,McQuade, D. Tyler,Opatz, Till

, p. 5519 - 5526 (2019)

There is an urgent demand for 5-fluorocytosine (5-FC) due to its activity against HIV-induced fungal infections as well as its use as a key intermediate in the synthesis of the clinically highly important anti-HIV drug emtricitabine (FTC). We report a simple, low-cost five steps synthesis of 5-FC starting from chloroacetamide. Overall yields up to 46 % were achieved and the route is devoid of any chromatographic purifications. The previously unknown key intermediate (Z)-2-cyano-2-fluoroethenolate is obtained through a Claisen-type condensation from fluoroacetonitrile. As the direct cyclization with urea only gave poor yields, 5-fluoro-2-methoxypyrimidin-4-amine, 5-fluoro-2-(methylsulfanyl)pyrimidin-4-amine and 5-fluoropyrimidine-2,4-diamine served as synthetic intermediates.

2-CYANO-2-FLUOROETHENOLATE SALTS (CFES): VERSITILE ACTIVE PHARMACEUTICAL INTERMEDIATES

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Paragraph 0010, (2020/08/30)

The present invention relates to new enolate structures with utility as active pharmaceutical intermediates for the preparation of efficacious drugs such as those derived from 5-fluorocytosine (5-FC).

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