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[5-(4-ethoxy-3,5-dimethoxyphenyl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid is a complex organic molecule characterized by a 1,2,4-triazole core with a sulfanyl acetic acid side chain and a phenyl group featuring two methoxy and one ethoxy substituents. [5-(4-ethoxy-3,5-dimethoxyphenyl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid holds potential as a pharmacological agent due to its unique molecular structure and functional groups, which may endow it with a range of biological activities, including antibiotic, antifungal, or anticancer properties. Its intriguing characteristics make it a promising candidate for further exploration in medicinal chemistry and drug development.

77803-57-7

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77803-57-7 Usage

Uses

Used in Pharmaceutical Industry:
[5-(4-ethoxy-3,5-dimethoxyphenyl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid is used as a potential pharmacological agent for its possible antibiotic, antifungal, or anticancer properties. [5-(4-ethoxy-3,5-dimethoxyphenyl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid's unique molecular structure and functional groups make it a candidate for further research and development in the creation of new drugs to combat various diseases.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [5-(4-ethoxy-3,5-dimethoxyphenyl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid serves as a subject of study for understanding its biological activities and potential applications. [5-(4-ethoxy-3,5-dimethoxyphenyl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid's structure and functional groups may provide insights into the design of new drugs with improved efficacy and selectivity.
Used in Drug Development:
[5-(4-ethoxy-3,5-dimethoxyphenyl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid is utilized in drug development as a starting point for the synthesis of new compounds with potential therapeutic applications. Its molecular structure and functional groups can be modified to optimize pharmacokinetic and pharmacodynamic properties, leading to the creation of more effective drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 77803-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,0 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77803-57:
(7*7)+(6*7)+(5*8)+(4*0)+(3*3)+(2*5)+(1*7)=157
157 % 10 = 7
So 77803-57-7 is a valid CAS Registry Number.

77803-57-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[5-(4-ethoxy-3,5-dimethoxyphenyl)-1H-1,2,4-triazol-3-yl]sulfanyl]acetic acid

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:77803-57-7 SDS

77803-57-7Relevant academic research and scientific papers

Synthesis of carboxyalkylthio-triazoles and bicyclic derivatives with antiinflammatory and analgesic activity

Mazzone,Pignatello,Mazzone,Panico,Barbera,Catti,Chiechio,Arrigo-Reina,Castorina,Russo

, p. 149 - 169 (2007/10/02)

3-Carboxyalkylthio derivatives of 5-alkoxyphenyl-1,2,4-triazole were prepared, performing some substitutions both on carboxyalkyl chain, by lengthening it or introducing substituents with increasing molecular weight in α- at the carboxy group, and on N-4

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