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1H-Imidazole-5-carbonylchloride,1-methyl-4-nitro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61982-14-7

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61982-14-7 Usage

Appearance

Yellow crystalline solid The compound is a yellow solid with a crystalline structure.

Molecular weight

198.58 g/mol The molecular weight of the compound is approximately 198.58 grams per mole.

Derivative

Carbonylchloride derivative of 1-methyl-4-nitroimidazole 1H-Imidazole-5-carbonylchloride,1-methyl-4-nitro-(9CI) is derived from 1-methyl-4-nitroimidazole by the addition of a carbonylchloride group.

Usage

Organic synthesis and pharmaceutical research The compound is commonly used as a building block in the synthesis of various heterocyclic compounds and pharmaceutical intermediates.

Structural features

Imidazole and nitro groups The presence of both imidazole and nitro groups in the structure makes the compound versatile for various chemical reactions and applications.

Toxicity

Likely toxic The compound is potentially toxic, and proper safety measures should be taken when handling it in the laboratory.

Check Digit Verification of cas no

The CAS Registry Mumber 61982-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,8 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61982-14:
(7*6)+(6*1)+(5*9)+(4*8)+(3*2)+(2*1)+(1*4)=137
137 % 10 = 7
So 61982-14-7 is a valid CAS Registry Number.

61982-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-5-nitroimidazole-4-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 3-Methyl-5-nitro-3H-imidazol-4-carbonylchlorid

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:61982-14-7 SDS

61982-14-7Relevant academic research and scientific papers

AROMATIC DERIVATIVES, PREPARATION METHODS, AND MEDICAL USES THEREOF

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Paragraph 0151; 0154, (2020/09/19)

The present disclosure relates generally to aromatic derivatives that are inhibitors of FGFR4 and are useful in treating FGFR4-associated diseases or conditions. Compositions containing the compounds of the present disclosure are also provided.

SULFONAMIDE DERIVATIVE AND MEDICINAL USE THEREOF

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Paragraph 0169, (2015/02/25)

Provided are sulfonamide derivatives of a specific chemical structure in which a sulfonamide group having, as a substituent, a phenyl group or a heterocyclic group having a hetero atom(s) as a constituent element(s) is present at its terminal, and pharmaceutically acceptable salts thereof. These compounds are novel compounds having excellent α4 integrin-inhibitory action.

ortho-Substituted azoles as selective and dual inhibitors of VEGF receptors 1 and 2

Kiselyov, Alexander S.,Piatnitski, Evgueni L.,Samet, Alexander V.,Kisliy, Victor P.,Semenov, Victor V.

, p. 1369 - 1375 (2007/10/03)

We have developed a series of novel potent ortho-substituted azole derivatives active against kinases VEGFR-1 and VEGFR-2. Both specific and dual ATP-competitive inhibitors of VEGFR-2 were identified. Kinase activity and selectivity could be controlled by varying the arylamido substituents at the azole ring. The most specific molecule (17) displayed >10-fold selectivity for VEGFR-2 over VEGFR-1. Compound activities in enzymatic and cell-based assays were in the range of activities for reported clinical and development candidates (IC50 30 × 10-5 cm/min) is indicative of their potential for intestinal absorption upon oral administration.

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