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5-Cyclopropyl-1,2,4-triazol-3-ylamine is an organic compound and a triazole derivative characterized by the presence of a cyclopropyl ring attached to a triazole ring and an amine group. 5-Cyclopropyl-1,2,4-triazol-3-ylamine is recognized for its potential in pharmaceutical research, where it can serve as a building block for the synthesis of biologically active molecules. The triazole moiety is known for its diverse pharmacological properties, and the cyclopropyl group adds structural diversity, potentially enhancing the compound's biological activity.

502546-41-0

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502546-41-0 Usage

Uses

Used in Pharmaceutical Research:
5-Cyclopropyl-1,2,4-triazol-3-ylamine is used as a building block for creating biologically active molecules due to its triazole core and cyclopropyl group, which contribute to a wide range of pharmacological activities and structural diversity.
Used in Drug Development:
In the pharmaceutical industry, 5-Cyclopropyl-1,2,4-triazol-3-ylamine is utilized for the development of new drugs targeting various medical conditions. Its unique structure allows for the modulation of biological activity, making it a valuable component in the creation of novel therapeutic agents.
Used in Materials Science:
5-Cyclopropyl-1,2,4-triazol-3-ylamine's structure also suggests potential applications in materials science, where it could be explored for its properties in different chemical research areas, contributing to the advancement of material technologies.
While the provided materials do not specify distinct applications in various industries beyond pharmaceutical research and drug development, the compound's versatility implies that it could be adapted for use in other sectors where novel chemical structures are of interest.

Check Digit Verification of cas no

The CAS Registry Mumber 502546-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,5,4 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 502546-41:
(8*5)+(7*0)+(6*2)+(5*5)+(4*4)+(3*6)+(2*4)+(1*1)=120
120 % 10 = 0
So 502546-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N4/c6-5-7-4(8-9-5)3-1-2-3/h3H,1-2H2,(H3,6,7,8,9)

502546-41-0SDS

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-cyclopropyl-1H-1,2,4-triazol-3-amine

1.2 Other means of identification

Product number -
Other names 5-cyclopropyl-4h-1,2,4-triazol-3-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:502546-41-0 SDS

502546-41-0Relevant academic research and scientific papers

Aminoazabenzimidazoles, a Novel Class of Orally Active Antimalarial Agents

Hameed P, Shahul,Chinnapattu, Murugan,Shanbag, Gajanan,Manjrekar, Praveena,Koushik, Krishna,Raichurkar, Anandkumar,Patil, Vikas,Jatheendranath, Sandesh,Rudrapatna, Suresh S.,Barde, Shubhada P.,Rautela, Nikhil,Awasthy, Disha,Morayya, Sapna,Narayan, Chandan,Kavanagh, Stefan,Saralaya, Ramanatha,Bharath, Sowmya,Viswanath, Pavithra,Mukherjee, Kakoli,Bandodkar, Balachandra,Srivastava, Abhishek,Panduga, Vijender,Reddy, Jitender,Prabhakar,Sinha, Achyut,Jiménez-Díaz, María Belén,Martínez, María Santos,Angulo-Barturen, I?igo,Ferrer, Santiago,Sanz, Laura María,Gamo, Francisco Javier,Duffy, Sandra,Avery, Vicky M.,Magistrado, Pamela A.,Lukens, Amanda K.,Wirth, Dyann F.,Waterson, David,Balasubramanian,Iyer, Pravin S.,Narayanan, Shridhar,Hosagrahara, Vinayak,Sambandamurthy, Vasan K.,Ramachandran, Sreekanth

supporting information, p. 5702 - 5713 (2014/08/05)

Whole-cell high-throughput screening of the AstraZeneca compound library against the asexual blood stage of Plasmodium falciparum (Pf) led to the identification of amino imidazoles, a robust starting point for initiating a hit-to-lead medicinal chemistry effort. Structure-activity relationship studies followed by pharmacokinetics optimization resulted in the identification of 23 as an attractive lead with good oral bioavailability. Compound 23 was found to be efficacious (ED90 of 28.6 mg·kg-1) in the humanized P. falciparum mouse model of malaria (Pf/SCID model). Representative compounds displayed a moderate to fast killing profile that is comparable to that of chloroquine. This series demonstrates no cross-resistance against a panel of Pf strains with mutations to known antimalarial drugs, thereby suggesting a novel mechanism of action for this chemical class.

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