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(2-METHYL-4-NITRO-IMIDAZOL-1-YL)-ACETIC ACID HYDRAZIDE, also known as N-methylhydrazinecarboximidamide, is a hydrazide derivative of imidazole, a heterocyclic organic compound. It has a nitro group and a methyl group attached to the imidazole ring, making it a valuable intermediate in the production of various organic compounds. Its unique structure and reactivity also make it a promising candidate for pharmaceutical and chemical research.

93637-76-4

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93637-76-4 Usage

Uses

Used in Pharmaceutical Research:
(2-METHYL-4-NITRO-IMIDAZOL-1-YL)-ACETIC ACID HYDRAZIDE is used as a precursor in the synthesis of various pharmaceutical drugs due to its unique structure and reactivity.
Used in Chemical Research:
(2-METHYL-4-NITRO-IMIDAZOL-1-YL)-ACETIC ACID HYDRAZIDE is used as a reagent in chemical reactions, contributing to the development of new organic compounds.
Used in Medicinal Chemistry:
(2-METHYL-4-NITRO-IMIDAZOL-1-YL)-ACETIC ACID HYDRAZIDE is used as a valuable intermediate in the production of a range of organic compounds, potentially leading to the discovery of new drugs and therapeutic agents.
Used in Drug Development:
(2-METHYL-4-NITRO-IMIDAZOL-1-YL)-ACETIC ACID HYDRAZIDE may have potential uses in the field of medicinal chemistry and drug development, given its unique structure and reactivity, which can be harnessed to create novel pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 93637-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,3 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93637-76:
(7*9)+(6*3)+(5*6)+(4*3)+(3*7)+(2*7)+(1*6)=164
164 % 10 = 4
So 93637-76-4 is a valid CAS Registry Number.

93637-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Imidazole-1-acetic acid, 2-methyl-4-nitro-, hydrazide

1.2 Other means of identification

Product number -
Other names 2-(2-methyl-4-nitro-1H-imidazol-1-yl)acetohydrazide

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:93637-76-4 SDS

93637-76-4Relevant academic research and scientific papers

Synthesis and anti-helicobacter pylori activity of (4-nitro-1- imidazolylmethyl)-1,2,4-triazoles, 1,3,4-thiadiazoles, and 1,3,4-oxadiazoles

Tafti, Asal Fallah,Akbarzadeh, Tahmineh,Saniee, Parastoo,Siavoshi, Farideh,Shafiee, Abbas,Foroumadi, Alireza

experimental part, p. 307 - 316 (2011/12/16)

A series of [(4-nitro-1 H-imidazol-1-yl) methyl]-1,2,4-triazoles and 1,3,4-thiadiazoles were prepared and evaluated for their activity against sensitive and resistant H. pylori strains. Study of the structure-activity relationship of these series of compounds indicated that the type of nitroimidazole moiety and the pendent group on the heteroaryl analog dramatically impact the anti-H. pylori activity. In triazole series, compound 5d, containing a 4-methyl phenyl group on the triazole ring, was the most potent compound tested against both metronidazole-sensitive and-resistant strains at a concentration of 8 μg. TUeBITAK.

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