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[5-(3,4-DIMETHOXY-PHENYL)-4-PHENYL-4 H-[1,2,4]TRIAZOL-3-YLSULFANYL]-ACETIC ACID is a complex chemical compound featuring a 1,2,4-triazole ring with a phenyl and dimethoxy-phenyl group attached to it. It also contains a sulfanyl group and an acetic acid moiety, which may contribute to its potential biological activities. [5-(3,4-DIMETHOXY-PHENYL)-4-PHENYL-4 H-[1,2,4]TRIAZOL-3-YLSULFANYL]-ACETIC ACID holds promise in medicinal chemistry for various applications, including its use as a drug or a lead compound for further drug development. However, more research is necessary to fully comprehend its properties and potential uses.

91759-73-8

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91759-73-8 Usage

Uses

Used in Pharmaceutical Industry:
[5-(3,4-DIMETHOXY-PHENYL)-4-PHENYL-4 H-[1,2,4]TRIAZOL-3-YLSULFANYL]-ACETIC ACID is used as a potential drug or lead compound for the development of new medications due to its unique chemical structure and potential biological activities. Its application in this industry is driven by the need for novel compounds that can address various health conditions and diseases.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [5-(3,4-DIMETHOXY-PHENYL)-4-PHENYL-4 H-[1,2,4]TRIAZOL-3-YLSULFANYL]-ACETIC ACID serves as a valuable compound for further research and development. Its unique structure and potential biological activities make it an interesting candidate for exploring new therapeutic approaches and understanding its interactions with biological targets.
Used in Drug Development:
[5-(3,4-DIMETHOXY-PHENYL)-4-PHENYL-4 H-[1,2,4]TRIAZOL-3-YLSULFANYL]-ACETIC ACID is used as a starting point for drug development, where its properties and potential uses are further investigated and optimized. This process involves extensive testing and modification to enhance its efficacy, safety, and pharmacokinetic profile, ultimately aiming to develop a new drug with improved therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 91759-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91759-73:
(7*9)+(6*1)+(5*7)+(4*5)+(3*9)+(2*7)+(1*3)=168
168 % 10 = 8
So 91759-73-8 is a valid CAS Registry Number.

91759-73-8SDS

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 Acetic acid, 2-[[5-(3,4-dimethoxyphenyl)-4-phenyl-4H-1,2,4-triazol-3-yl]thio]-

1.2 Other means of identification

Product number -
Other names Acetic acid, [[5-(3,4-dimethoxyphenyl)-4-phenyl-4H-1,2,4-triazol-3-yl]thio]-

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:91759-73-8 SDS

91759-73-8Downstream Products

91759-73-8Relevant academic research and scientific papers

Synthesis of 5-Aryl-2H-tetrazoles, 5-Aryl-2H-tetrazole-2-acetic Acids, and acetic Acids as Possible Superoxide Scavengers and Antiinflammatory Agents

Maxwell, James R.,Wasdahl, Dan A.,Wolfson, Alan C.,Stenberg, Virgil I.

, p. 1565 - 1570 (2007/10/02)

A series of 5-aryl-2H-tetrazoles, 5-aryl-2H-tetrazole-2-acetic acids, and acetic acids were synthesized and tested in vitro for superoxide scavenging activity, in vivo in the carrageenan-induced rat paw edema assay, and in the reverse passive Arthus reaction.The hydroxy-substituted compounds were effective as in vitro scavengers of superoxide but were not effective as in vivo antiinflammatory agents.

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