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3-[(4-Methoxybenzyl)thio]-1H-1,2,4-triazole is a chemical compound characterized by its molecular formula C10H10N2OS. It is a triazole derivative featuring a sulfur atom connected to a benzyl group with a methoxy substituent. 3-[(4-METHOXYBENZYL)THIO]-1H-1,2,4-TRIAZOLE is recognized for its potential applications in coordination chemistry as a ligand and in organic synthesis as a building block. Additionally, it demonstrates antifungal and antimicrobial properties, which are of interest for both pharmaceutical and agricultural sectors. The 1,2,4-triazole component of the molecule is a prevalent pharmacophore, suggesting its significance as a scaffold for the development of novel pharmaceutical agents.

17357-75-4

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17357-75-4 Usage

Uses

Used in Coordination Chemistry:
3-[(4-METHOXYBENZYL)THIO]-1H-1,2,4-TRIAZOLE is used as a ligand for its ability to form stable complexes with metal ions, which is crucial in the study and application of coordination compounds.
Used in Organic Synthesis:
In the field of organic synthesis, 3-[(4-METHOXYBENZYL)THIO]-1H-1,2,4-TRIAZOLE serves as a valuable building block, contributing to the creation of a diverse range of organic compounds.
Used in Pharmaceutical Applications:
3-[(4-METHOXYBENZYL)THIO]-1H-1,2,4-TRIAZOLE is used as a potential pharmaceutical agent due to its antifungal and antimicrobial activities, which can be harnessed in the development of new treatments for various infections.
Used in Agricultural Applications:
In agriculture, 3-[(4-METHOXYBENZYL)THIO]-1H-1,2,4-TRIAZOLE is utilized for its antifungal and antimicrobial properties, potentially serving as a component in fungicides and antimicrobial agents to protect crops.
Used in Drug Development:
3-[(4-METHOXYBENZYL)THIO]-1H-1,2,4-TRIAZOLE is used as a scaffold in drug development because of the 1,2,4-triazole moiety, which is a common pharmacophore, indicating its potential role in the creation of new pharmaceuticals with various therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17357-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,5 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17357-75:
(7*1)+(6*7)+(5*3)+(4*5)+(3*7)+(2*7)+(1*5)=124
124 % 10 = 4
So 17357-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3OS/c1-14-9-4-2-8(3-5-9)6-15-10-11-7-12-13-10/h2-5,7H,6H2,1H3,(H,11,12,13)

17357-75-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H50648)  3-(4-Methoxybenzylthio)-1H-1,2,4-triazole   

  • 17357-75-4

  • 250mg

  • 622.0CNY

  • Detail
  • Alfa Aesar

  • (H50648)  3-(4-Methoxybenzylthio)-1H-1,2,4-triazole   

  • 17357-75-4

  • 1g

  • 2368.0CNY

  • Detail

17357-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(4-methoxyphenyl)methylsulfanyl]-1H-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 3-(4-Methoxybenzylthio)-1H-1,2,4-triazole

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:17357-75-4 SDS

17357-75-4Downstream Products

17357-75-4Relevant academic research and scientific papers

Synthesis and antimycobacterial activity of 1,2,4-triazole 3-benzylsulfanyl derivatives

Klimesova, Vera,Zahajska, Lenka,Waisser, Karel,Kaustova, Jarmila,Moellmann, Ute

, p. 279 - 288 (2007/10/03)

Series of 3-benzylsulfanyl derivatives of 1,2,4-triazole and 4-methyl-1,2,4-triazole were synthesized by alkylation of starting triazole-3-thiol with appropriately substituted benzyl halide. All members of the set were evaluated for in vitro antimycobacte

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