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2-Iodo-4-methylimidazole, a chemical compound with the molecular formula C4H5IN2, is a derivative of imidazole. It is characterized by the presence of an iodo group, which makes it a valuable reagent for organic synthesis, especially in the production of heterocyclic compounds. 2-Iodo-4-methylimidazole is also utilized as a building block in the preparation of various specialty chemicals, including corrosion inhibitors and dyes. Due to its wide range of potential applications, 2-Iodo-4-methylimidazole is of significant interest to researchers and industrial chemists. However, it is crucial to handle this chemical with care, as it may pose health and environmental risks.

73746-43-7

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73746-43-7 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Iodo-4-methylimidazole is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agricultural Chemical Production:
2-Iodo-4-methylimidazole is also utilized as an intermediate in the production of agricultural chemicals, contributing to the development of more effective and targeted pest control solutions.
Used in Organic Synthesis:
2-Iodo-4-methylimidazole is used as a reagent in organic synthesis, particularly for the production of heterocyclic compounds. Its iodo group facilitates various chemical reactions, making it a versatile building block in the synthesis of complex organic molecules.
Used in Corrosion Inhibitor Preparation:
In the chemical industry, 2-Iodo-4-methylimidazole is used as a building block for the preparation of corrosion inhibitors. These inhibitors are essential in protecting materials from degradation, extending their service life and improving their performance in various applications.
Used in Dye Manufacturing:
2-Iodo-4-methylimidazole is also employed in the manufacturing of dyes, where its unique chemical properties contribute to the development of new dyes with specific color characteristics and application properties.

Check Digit Verification of cas no

The CAS Registry Mumber 73746-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,4 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73746-43:
(7*7)+(6*3)+(5*7)+(4*4)+(3*6)+(2*4)+(1*3)=147
147 % 10 = 7
So 73746-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H5IN2/c1-3-2-6-4(5)7-3/h2H,1H3,(H,6,7)

73746-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-4-methyl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-iodo-5-methyl-1H-imidazole

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:73746-43-7 SDS

73746-43-7Upstream product

73746-43-7Downstream Products

73746-43-7Relevant academic research and scientific papers

Kinetics of Iodination of 4-Methylimidazole and 2-Methylimidazole

Vaughan, John D.,Vaughan, Virginia L.,Daly, Steven S.,Smith, William A.

, p. 3108 - 3111 (1980)

Since the rate law for the diiodination of imidazole provides information on the iodination of C4(5) but not C2 in the imidazole ring, we have investigated the kinetics of iodination of the two positions separately in 2-methylimidazole and 4-methylimidazole, respectively.The observed rate laws for the methylimidazoles exhibited hydrogen ion dependencies that differed from that of imidazole; the iodinations of all three substrates were base catalyzed, but like imidazole, 2-methylimidazole undergoes uncatalyzed iodination, while 4-methylimidazole does not.The overall rate of iodination of 4-methylimidazole was faster than that of 2-methylimidazole which was faster than that of imidazole.

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