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1H-Benzimidazole, 2-[(2,4-dinitrophenyl)thio]is a chemical compound that features a benzimidazole ring with a 2-[(2,4-dinitrophenyl)thio] group attached to it. This yellow crystalline substance is known for its strong chemical reactivity, making it a valuable reactive intermediate in organic reactions. Its diverse applications stem from its chemical and biological properties, which include potential antimicrobial and anticancer activities.

19919-16-5

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19919-16-5 Usage

Uses

Used in Organic Synthesis:
1H-Benzimidazole, 2-[(2,4-dinitrophenyl)thio]is used as a reactive intermediate in the synthesis of various organic compounds, contributing to the creation of a wide range of chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1H-Benzimidazole, 2-[(2,4-dinitrophenyl)thio]is utilized in the development and manufacturing of drugs, capitalizing on its chemical reactivity and potential pharmacological properties.
Used in Agrochemical Production:
1H-Benzimidazole, 2-[(2,4-dinitrophenyl)thio]also finds application in the agrochemical sector, where it is employed in the production of pesticides and other agricultural chemicals to help improve crop protection and yield.
Used in Dye Manufacturing:
1H-Benzimidazole, 2-[(2,4-dinitrophenyl)thio]is used as a key component in the manufacturing of dyes, contributing to the coloration and quality of various products.
Used in Antimicrobial Applications:
Due to its potential antimicrobial properties, 1H-Benzimidazole, 2-[(2,4-dinitrophenyl)thio]is studied for use in applications that require the inhibition of microbial growth, such as in medical and industrial settings.
Used in Anticancer Research:
1H-Benzimidazole, 2-[(2,4-dinitrophenyl)thio]is also being investigated for its potential anticancer properties, with the aim of developing new therapeutic agents for the treatment of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 19919-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,1 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19919-16:
(7*1)+(6*9)+(5*9)+(4*1)+(3*9)+(2*1)+(1*6)=145
145 % 10 = 5
So 19919-16-5 is a valid CAS Registry Number.

19919-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-dinitrophenyl)sulfanyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 1-benzimidazol-2-ylthio-2,4-dinitrobenzene

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:19919-16-5 SDS

19919-16-5Relevant academic research and scientific papers

Regioselective synthesis of isoxazole-mercaptobenzimidazole hybrids and their in vivo analgesic and anti-inflammatory activity studies

Kankala, Shravankumar,Kankala, Ranjith Kumar,Gundepaka, Prasad,Thota, Niranjan,Nerella, Srinivas,Gangula, Mohan Rao,Guguloth, Hanmanthu,Kagga, Mukkanti,Vadde, Ravinder,Vasam, Chandra Sekhar

supporting information, p. 1306 - 1309 (2013/03/14)

Regioselective synthesis of isoxazole-mercaptobenzimidazole hybrids and their efficiency in in vivo analgesic and anti-inflammatory activity was described. A comparison of structure-activity relationship for there compounds was also emphasized.

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