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1H-Benzimidazol-2-amine, 4-methyl(9CI) is a chemical compound belonging to the benzimidazole class, characterized by the molecular formula C8H9N3. It features a methyl group at the 4-position of the benzimidazole ring, which contributes to its diverse pharmacological activities. 1H-Benzimidazol-2-amine, 4-methyl(9CI) has demonstrated biological activities, including antimicrobial and antifungal properties, and has been considered as a potential building block for synthesizing other biologically active compounds. Its potential applications span across various fields such as medicine, agriculture, and material science.

171082-91-0

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171082-91-0 Usage

Uses

Used in Pharmaceutical Industry:
1H-Benzimidazol-2-amine, 4-methyl(9CI) is used as a pharmaceutical compound for its antimicrobial and antifungal properties, making it a candidate for developing new drugs to combat infections caused by various microorganisms.
Used in Agricultural Industry:
In agriculture, 1H-Benzimidazol-2-amine, 4-methyl(9CI) is utilized as an antimicrobial and antifungal agent to protect crops from diseases and pests, thereby enhancing crop yield and quality.
Used in Material Science:
1H-Benzimidazol-2-amine, 4-methyl(9CI) serves as a building block in material science for the synthesis of other biologically active compounds, contributing to the development of new materials with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 171082-91-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,0,8 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 171082-91:
(8*1)+(7*7)+(6*1)+(5*0)+(4*8)+(3*2)+(2*9)+(1*1)=120
120 % 10 = 0
So 171082-91-0 is a valid CAS Registry Number.

171082-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1H-benzimidazol-2-amine

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazol-2-amine,4-methyl

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:171082-91-0 SDS

171082-91-0Downstream Products

171082-91-0Relevant academic research and scientific papers

MRGX Receptor Antagonists

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Paragraph 0277; 0287; 0286, (2021/05/07)

The invention relates to a method for preventing or treating a disease or disorder that is associated with the MrgX2 receptor. The invention also relates to MrgX2 antagonists and physiologically acceptable salts thereof. The invention also relates to pharmaceutical compositions and dosage forms comprising an MrgX2 antagonist.

Inhibition and Dispersion of Bacterial Biofilms with 2-Aminobenzimidazole Derivatives

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Paragraph 0216; 0217; 0232; 0233, (2013/06/05)

Compounds described herein inhibit biofilm formation or disperse pre-formed biofilms of Gram-negative bacteria. Biofilm-inhibitory compounds can be encapsulated or contained in a polymer matrix for controlled release. Coatings, films, multilayer films, hydrogels, microspheres and nanospheres as well as pharmaceutical compositions and disinfecting compositions containing biofilm-inhibitory compounds are also provided. Methods for inhibiting formation of biofilms or dispersing already formed biofilms are provided. Methods for treating infections of gram-negative bacteria which form biofilms, particularly those of Pseudomonas and more particularly P. aeruginosa.

2-aminobenzimidazole derivatives strongly inhibit and disperse Pseudomonas aeruginosa biofilms

Frei, Reto,Breitbach, Anthony S.,Blackwell, Helen E.

supporting information; experimental part, p. 5226 - 5229 (2012/07/03)

Bacterial biofilms are exceptionally difficult to clear using traditional antibiotics and constitute a significant health threat. 2-Aminobenzimidazole derivatives (see scheme) are capable of strongly inhibiting the growth of and dispersing Pseudomonas aeruginosa biofilms. These molecules were found to modulate quorum sensing in reporter strains, and represent some of strongest P. aeruginosa biofilm inhibitors known. Copyright

Catalyst-controlled chemoselective arylation of 2-aminobenzimidazoles

Ueda, Satoshi,Buchwald, Stephen L.

supporting information, p. 10364 - 10367 (2012/11/13)

What N would you like? The chemoselective and complementary Pd- and Cu-catalyzed N-arylation of 2-aminobenzimidazoles is described. Selective N-arylation of the amino group was achieved with a Pd-catalyzed method, while selective N-arylation of azole nitrogen was achieved with a Cu-catalyzed procedure (see scheme). Copyright

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