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1H-Benzimidazole-5-carboxylic acid, 2-methyl-hydrazide (9CI) is a chemical compound with the molecular formula C9H10N4O2. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to an imidazole ring. The 2-methyl group in 1H-Benzimidazole-5-carboxylicacid,2-methyl-,hydrazide(9CI) is attached to the benzene ring, and the hydrazide functional group is present at the 5-position of the benzimidazole ring. 1H-Benzimidazole-5-carboxylicacid,2-methyl-,hydrazide(9CI) is known for its potential applications in pharmaceuticals and medicinal chemistry, particularly as a building block for the synthesis of various bioactive molecules. Its unique structure and properties make it a valuable intermediate in the development of new drugs and therapeutic agents.

713-17-7

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713-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 713-17-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 713-17:
(5*7)+(4*1)+(3*3)+(2*1)+(1*7)=57
57 % 10 = 7
So 713-17-7 is a valid CAS Registry Number.

713-17-7SDS

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 2-methyl-1H-benzimidazole-5-carbohydrazide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:713-17-7 SDS

713-17-7Downstream Products

713-17-7Relevant academic research and scientific papers

Synthesis and biological evaluation of 2-methyl-1H-benzimidazole-5-carbohydrazides derivatives as modifiers of redox homeostasis of Trypanosoma cruzi

Melchor-Doncel de la Torre, Silvia,Vázquez, Citlali,González-Chávez, Zabdi,Yépez-Mulia, Lilián,Nieto-Meneses, Rocío,Jasso-Chávez, Ricardo,Saavedra, Emma,Hernández-Luis, Francisco

supporting information, p. 3403 - 3407 (2017/07/07)

Twelve novel benzimidazole derivatives were synthesized and their in vitro activities against epimastigotes of Trypanosoma cruzi were evaluated. Two derivatives (6 and 7), which have 4-hydroxy-3-methoxyphenyl moiety in their structures, proved to be the m

Synthesis and antibacterial activity of novel 4″-O-benzimidazolyl clarithromycin derivatives

Cong, Chao,Wang, Haiyang,Hu, Yue,Liu, Chen,Ma, Siti,Li, Xin,Cao, Jichao,Ma, Shutao

, p. 3105 - 3111 (2011/07/08)

Novel 4″-O-benzimidazolyl clarithromycin derivatives were designed, synthesized and evaluated for their in vitro antibacterial activities. These benzimidazolyl derivatives exhibited excellent activity against erythromycin-susceptible strains better than the references, and some of them showed greatly improved activity against erythromycin-resistant strains. Compounds 16 and 17, which have the terminal 2-(4-methylphenyl)benzimidazolyl and 2-(2-methoxyphenyl)benzimidazolyl groups on the C-4″ bishydrazide side chains, were the most active against erythromycin-resistant Staphylococcus pneumoniae expressing the erm gene and the mef gene. In addition, compound 17 exhibited the highest activity against erythromycin-susceptible S. pneumoniae ATCC49619 and Staphylococcus aureus ATCC25923 as well. It is worth noting that the 4″-O-(2-aryl)benzimidazolyl derivatives show higher activity against erythromycin-susceptible and erythromycin-resistant strains than the 4″-O-(2-alkyl)benzimidazolyl derivatives.

New transition metal ion complexes with benzimidazole-5-carboxylic acid hydrazides with antitumor activity

Galal, Shadia A.,Hegab, Khaled H.,Kassab, Ahmed S.,Rodriguez, Mireya L.,Kerwin, Sean M.,El-Khamry, Abdel-Mo'men A.,El Diwani, Hoda I.

experimental part, p. 1500 - 1508 (2009/07/11)

Metal complexes of 2-methyl-1H-benzimidazole-5-carboxylic acid hydrazide (4a; L1) and its Schiff base 2-methyl-N-(propan-2-ylidene)-1H-benzimidazole-5-carbohydrazide (5a; L2) with transition metal ions e.g., copper, silver, nickel, i

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