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71759-88-1

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71759-88-1 Usage

Description

5-IODO-1-METHYL-1H-IMIDAZOLE, with the molecular formula C4H5IN2, is a chemical compound belonging to the class of organic compounds known as imidazoles. It is characterized by an iodine atom attached at the fifth position of the imidazole ring and a methyl group attached at the first position. Recognized by its IUPAC name as 5-iodo-1-methyl-1H-imidazole, this substance is known for its valuable properties and is used across various fields. However, it requires careful handling due to potential skin, eye irritation, and complications if ingested, necessitating proper safety measures during its use.

Uses

Used in Pharmaceutical Industry:
5-IODO-1-METHYL-1H-IMIDAZOLE is used as an active pharmaceutical ingredient for the development of medications, leveraging its chemical properties to target specific biological processes and conditions.
Used in Chemical Research:
5-IODO-1-METHYL-1H-IMIDAZOLE is used as a research compound in the field of organic chemistry, allowing scientists to study its reactivity, structure, and potential applications in the synthesis of other compounds.
Used in Material Science:
5-IODO-1-METHYL-1H-IMIDAZOLE is used as a component in the development of new materials, such as sensors or catalysts, due to its unique chemical properties and potential interactions with other molecules.
Used in Diagnostic Applications:
5-IODO-1-METHYL-1H-IMIDAZOLE is used as a diagnostic agent in medical imaging, where its chemical properties may enhance the visibility of specific tissues or structures within the body.
Used in Environmental Applications:
5-IODO-1-METHYL-1H-IMIDAZOLE is used in environmental monitoring and remediation efforts, potentially serving as a tracer or indicator for the presence of certain contaminants or pollutants.

Check Digit Verification of cas no

The CAS Registry Mumber 71759-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,7,5 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71759-88:
(7*7)+(6*1)+(5*7)+(4*5)+(3*9)+(2*8)+(1*8)=161
161 % 10 = 1
So 71759-88-1 is a valid CAS Registry Number.

71759-88-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H56932)  5-Iodo-1-methylimidazole, 97%   

  • 71759-88-1

  • 250mg

  • 449.0CNY

  • Detail
  • Alfa Aesar

  • (H56932)  5-Iodo-1-methylimidazole, 97%   

  • 71759-88-1

  • 1g

  • 1749.0CNY

  • Detail
  • Aldrich

  • (679739)  5-Iodo-1-methylimidazole  97%

  • 71759-88-1

  • 679739-250MG

  • 449.28CNY

  • Detail

71759-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Iodo-1-methyl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 5-iodo-1-methylimidazole

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:71759-88-1 SDS

71759-88-1Relevant articles and documents

PURINONES AS UBIQUITIN-SPECIFIC PROTEASE 1 INHIBITORS

-

Paragraph 00394, (2017/06/12)

The application relates to inhibitors of USP1 useful in the treatment of cancers, and other USP1 associated diseases and disorders, having the Formula: (I), where R1, R2, R3, R3', R4, R5, X1, X2, X3, X4, and n are described herein.

Development of a regioselective N-methylation of (benz)imidazoles providing the more sterically hindered isomer

Van Den Berge, Emilie,Robiette, Raphael

, p. 12220 - 12223 (2014/01/06)

An efficient and highly regioselective N-methylation of (NH)-(benz)imidazoles furnishing the sterically more hindered, less stable, and usually minor regioisomer has been developed. The methodology involves very mild reaction conditions and tolerates a wide range of functional groups.

A convenient synthesis of 1,4-disubstituted imidazoles

He, Yong,Chen, Yingzhong,Du, Hongwang,Schmid, Lesley A.,Lovely, Carl J.

, p. 5529 - 5532 (2007/10/03)

An efficient method for the regioselective protection of 4-alkyl-, 4-iodo, 4-vinylimidazoles has been developed via an alkylation-isomerization sequence with various imidazole-protecting groups. The initially formed mixture of 4/5-alkyl-, 4/5-iodo, and 4/5-vinylimidazoles are isomerized to the corresponding 4-isomers on treatment of a DMF solution with a small amount of RX and heating at 75°C.

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