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134717-73-0

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134717-73-0 Usage

Description

(5-(3-thienyl)tetrazol-1-yl)acetic acid is a chemical compound characterized by its molecular formula C9H8N4O2S. It is a tetrazole derivative featuring a thienyl group attached to the tetrazole ring, which endows the molecule with unique properties. (5-(3-thienyl)tetrazol-1-yl)acetic acid holds potential pharmacological properties and is considered for the development of new drugs. The combination of the tetrazole and thienyl moieties in its structure makes it a promising candidate for further exploration in medicinal chemistry and drug design.

Uses

Used in Pharmaceutical Development:
(5-(3-thienyl)tetrazol-1-yl)acetic acid is used as a chemical intermediate for the development of new drugs due to its potential pharmacological properties. The presence of the tetrazole and thienyl groups in the molecule may contribute to its therapeutic effects, making it a valuable compound for further research and development in the pharmaceutical industry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (5-(3-thienyl)tetrazol-1-yl)acetic acid is used as a compound of interest for studying its unique characteristics and potential applications. The tetrazole and thienyl moieties in its structure may offer novel insights into drug design and the development of more effective therapeutic agents.
Used in Drug Design:
(5-(3-thienyl)tetrazol-1-yl)acetic acid is utilized as a key component in drug design, where its unique structural features can be leveraged to create innovative and effective medications. (5-(3-thienyl)tetrazol-1-yl)acetic acid's potential pharmacological properties make it a valuable asset in the ongoing quest to develop new drugs with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 134717-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,7,1 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134717-73:
(8*1)+(7*3)+(6*4)+(5*7)+(4*1)+(3*7)+(2*7)+(1*3)=130
130 % 10 = 0
So 134717-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N4O2S/c12-6(13)3-11-7(8-9-10-11)5-1-2-14-4-5/h1-2,4H,3H2,(H,12,13)

134717-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-thiophen-3-yltetrazol-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 1H-Tetrazole-1-acetic acid,5-(3-thienyl)

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:134717-73-0 SDS

134717-73-0Upstream product

134717-73-0Downstream Products

134717-73-0Related news

Effect of a potent new aldose reductase inhibitor, (5-(3-thienyl)tetrazol-1-yl)acetic acid (TAT), on diabetic neuropathy in rats07/30/2019

(5-(3-Thienyl)tetrazol-1-yl)acetic acid (TAT), a novel potent aldose reductase inhibitor, was administered for 4 weeks to rats with streptozotocin-induced diabetes. Physiological and biochemical studies were subsequently conducted on rat nerve tissue and erythrocyte sorbitol content was estimate...detailed

134717-73-0Relevant articles and documents

TETRAZOLEACETIC ACID DERIVATIVES AND USE FOR ALDOSE REDUCTASE INHIBITORY ACTIVITY

-

, (2008/06/13)

A tetrazoleacetic acid derivative represented by the following general formula (I): [in Formula (I), R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a halogen atom, a haloalkyl group, a hydroxyl group, an alkoxy group, an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl sulfonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl group or an alkyl or aryl sulfinyl group; and X represents -O- or -S-] except for [5-(2-thienyl)tetrazol-1-yl] acetic acid, [5-(2-furyl)tetrazol-1-yl] acetic acid and ethyl esters thereof, or a salt thereof shows excellent aldose reductase inhibitory activity, has low toxicity to organisms and is quite effective as an essential component of a preventive medicine and/or remedy for diabetic complications.

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