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5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole is a complex organic compound with the molecular formula C11H9N3S and a molar mass of 215.27 g/mol. It is known for its solubility in benzene and ethanol. 5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole should be handled with caution due to its potential to irritate the respiratory system and eyes upon exposure.

172152-53-3

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172152-53-3 Usage

Uses

Used in Chemical Research:
5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole is used as a research compound for its unique chemical properties, contributing to the advancement of scientific knowledge in the field of chemistry.
Used in Pharmaceutical Development:
5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole is used as a potential pharmaceutical agent, given its complex structure and reactivity, which may offer new avenues for drug discovery and therapeutic applications.
Used in Industrial Applications:
5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole is used as a chemical intermediate in various industrial processes, where its specific properties can be harnessed to improve product performance or manufacturing efficiency.
Used in Material Science:
5-(1H-Pyrrol-1-yl)-2-mercaptobenzimidazole is used as a component in the development of new materials, such as polymers or composites, where its unique characteristics can enhance material properties like strength, flexibility, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 172152-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,1,5 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 172152-53:
(8*1)+(7*7)+(6*2)+(5*1)+(4*5)+(3*2)+(2*5)+(1*3)=113
113 % 10 = 3
So 172152-53-3 is a valid CAS Registry Number.

172152-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-pyrrol-1-yl-1,3-dihydrobenzimidazole-2-thione

1.2 Other means of identification

Product number -
Other names 5-(1H-pyrrole-1-yl)-2-mercaptobenzimidazole

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:172152-53-3 SDS

172152-53-3Relevant articles and documents

Diversified synthesis of novel quinoline and dibenzo thiazepine derivatives using known active intermediates

Sharada,Satyanarayana Reddy,Sammaiah,Sumalatha

, p. 7959 - 7966 (2013/09/23)

The novel drug development to control resisting infections in conventional drug therapy is a need of today. Few antiulcer relative derivatives developed by approaching convergent synthesis. The derivatives synthesized successfully are dibenzo thiazepine-pyridine (SLN11-SLN15) and benzimidazole-hydroquinoline based derivatives (SLN16-SLN20). It involved the coupling through microwave, sonication and conventional techniques at final step. The efficient technology identified as sonication technique basically time and yield. The reported compounds were structural characterized by elemental analysis and spectral studies such as 1H, 13C NMR and MS.

PROCESS FOR PREPARING INTERMEDIATE COMPOUND FOR SYNTHESIZING AN ANTIULCERANT

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Page/Page column 3, (2011/04/18)

The present invention relates a novel method of preparing an intermediate which is useful for synthesizing an antiulcerant. The present invention provides a method of preparing an intermediate of an antiulcerant which can obtain a high purity compound in high yield, with reduced production cost/time as compared to a conventional method.

PROCESS FOR PREPARING INTERMEDIATE COMPOUND FOR SYNTHESIZING AN ANTIULCERANT

-

Page 5-6, (2010/01/07)

The present invention relates a novel method of preparing an intermediate which is useful for synthesizing an antiulcerant. The present invention provides a method of preparing an intermediate of an antiulcerant which can obtain a high purity compound in high yield, with reduced production cost/time as compared to a conventional method.

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