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5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine is a chemical compound that belongs to the triazol-3-amine family. It is a derivative of the triazole ring system and contains a trifluoromethylphenyl group. 5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine is characterized by its potential applications in medicinal chemistry, particularly as a scaffold for the development of new drugs. The trifluoromethyl group imparts unique properties to molecules, enhancing their value in drug design, while the triazole ring system is known for its biological activity, making it a promising candidate for various therapeutic applications.

502686-01-3

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502686-01-3 Usage

Uses

Used in Medicinal Chemistry:
5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine is used as a scaffold in the development of new drugs due to its unique structural features and potential for imparting beneficial properties to pharmaceutical compounds.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine is used as a potential agent for the development of new antimicrobial drugs, leveraging the biological activity of the triazole ring system.
Used in Antifungal Applications:
5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine is utilized as a candidate for antifungal drug development, taking advantage of the triazole ring's known antifungal properties.
Used in Antiviral Applications:
5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine is considered for the development of antiviral medications, as the triazole ring system has been investigated for its antiviral properties.
Used in Anticancer Applications:
5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine is used as a potential anticancer agent, with the triazole ring system being explored for its ability to target and inhibit cancer cell growth.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine is used as a key intermediate in the synthesis of various therapeutic agents, capitalizing on its structural and functional attributes to create innovative medications with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 502686-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,6,8 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 502686-01:
(8*5)+(7*0)+(6*2)+(5*6)+(4*8)+(3*6)+(2*0)+(1*1)=133
133 % 10 = 3
So 502686-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3N4/c10-9(11,12)6-3-1-2-5(4-6)7-14-8(13)16-15-7/h1-4H,(H3,13,14,15,16)

502686-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[3-(Trifluoromethyl)phenyl]-1H-1,2,4-triazol-3-amine

1.2 Other means of identification

Product number -
Other names 3-[3-(trifluoromethyl)phenyl]-1H-1,2,4-triazol-5-amine

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:502686-01-3 SDS

502686-01-3Relevant academic research and scientific papers

A structure-activity relationship study of 1,2,4-triazolo[1,5-a][1,3,5] triazin-5,7-dione and its 5-thioxo analogues on anti-thymidine phosphorylase and associated anti-angiogenic activities

Bera, Hriday,Tan, Bee Jen,Sun, Lingyi,Dolzhenko, Anton V.,Chui, Wai-Keung,Chiu, Gigi Nagar Chee

, p. 325 - 334 (2013/10/01)

Thirty-three 1,2,4-triazolo[1,5-a][1,3,5]triazin-5,7-dione and its 5-thioxo analogues were designed and synthesized which contained different substituents at meta- and/or para-positions of 2-phenyl or 2-benzyl ring attached to the fused ring structure. Th

COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT

-

, (2012/02/01)

Compounds having activity as phosphate transport inhibitors, more specifically, inhibitors of intestinal apical membrane Na/phosphate co-transport, are disclosed. The compounds have the following structure (I): including stereoisomers, pharmaceutically ac

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