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5-Fluoropyrimidin-4-amine is a chemical compound belonging to the fluoropyrimidines class. It is a pyrimidine derivative characterized by the presence of a fluorine atom at the fifth carbon and an amino group at the fourth carbon. 5-fluoropyrimidin-4-amine has garnered interest in pharmaceutical research, particularly for its potential in developing antiviral and anticancer drugs due to its ability to inhibit the enzyme thymidylate synthase, which plays a crucial role in DNA synthesis.

811450-26-7

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811450-26-7 Usage

Uses

Used in Pharmaceutical Industry:
5-Fluoropyrimidin-4-amine is used as a pharmaceutical intermediate for the development of antiviral and anticancer drugs. Its application is based on its capacity to inhibit thymidylate synthase, an enzyme essential for DNA synthesis, thereby disrupting the growth and replication of cancer cells and potentially combating viral infections.
Used in Cancer Treatment:
5-Fluoropyrimidin-4-amine is utilized as an anticancer agent, targeting the disruption of DNA synthesis in cancer cells by inhibiting thymidylate synthase. This action can lead to the suppression of tumor growth and may be effective against a range of cancer types.
Used in Drug Development:
In the field of drug development, 5-fluoropyrimidin-4-amine serves as a key compound in the creation of new therapeutic agents. Its unique ability to target and inhibit a critical enzyme in DNA synthesis positions it as a promising candidate for further research and potential incorporation into novel medications aimed at treating cancer and viral diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 811450-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,1,4,5 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 811450-26:
(8*8)+(7*1)+(6*1)+(5*4)+(4*5)+(3*0)+(2*2)+(1*6)=127
127 % 10 = 7
So 811450-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H4FN3/c5-3-1-7-2-8-4(3)6/h1-2H,(H2,6,7,8)

811450-26-7SDS

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 5-Fluoropyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 5-FLUORO-PYRIMIDIN-4-YLAMINE

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:811450-26-7 SDS

811450-26-7Downstream Products

811450-26-7Relevant academic research and scientific papers

Synthesis of 4-amino-5-fluoropyrimidines and 5-amino-4-fluoropyrazoles from a β-fluoroenolate salt

Dietz, Jule-Philipp,Lucas, Tobias,Opatz, Till

, p. 445 - 450 (2020/03/27)

A synthesis of fluorinated pyrimidines under mild conditions from amidine hydrochlorides and the recently described potassium 2-cyano-2-fluoroethenolate was developed. A broad substrate scope was tested and mostly excellent yields were obtained. The synthesis of fluorinated aminopyrazoles from the same fluorinated precursor could be demonstrated but proceeded with lower efficiency.

Peptide deformylase inhibitors

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Page/Page column, (2014/12/09)

The present invention relates to a compound of Formula (I): or a pharmaceutically acceptable salt thereof, corresponding pharmaceutical compositions, compound preparation and treatment methods directed to bacterial infections and inhibition of bacterial peptide deformylase (PDF) activity.

PEPTIDE DEFORMYLASE INHIBITORS

-

Page/Page column, (2014/02/15)

The present invention relates to a compound of Formula (I): or a pharmaceutically acceptable salt thereof, corresponding pharmaceutical compositions, compound preparation and treatment methods directed to bacterial infections and inhi-bition of bacterial peptide deformylase (PDF) activity

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