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157255-72-6

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157255-72-6 Usage

General Description

2-Methyl-4-iodo-1-tritylimidazole is a chemical compound that belongs to the class of imidazoles. It is a white to off-white solid substance with a molecular formula of C21H17IN2 and a molecular weight of 422.28 g/mol. The compound is commonly used as a building block in the synthesis of various pharmaceutical compounds and organic materials. Its unique structure and properties make it suitable for use in the development of new and innovative products. The compound can be produced through various synthetic methods and is available for purchase from chemical suppliers.

Check Digit Verification of cas no

The CAS Registry Mumber 157255-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,2,5 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 157255-72:
(8*1)+(7*5)+(6*7)+(5*2)+(4*5)+(3*5)+(2*7)+(1*2)=146
146 % 10 = 6
So 157255-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C23H19IN2/c1-18-25-22(24)17-26(18)23(19-11-5-2-6-12-19,20-13-7-3-8-14-20)21-15-9-4-10-16-21/h2-17H,1H3

157255-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 4-iodo-2-methyl-1-tritylimidazole

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:157255-72-6 SDS

157255-72-6Relevant articles and documents

Important Hydrogen Bond Networks in Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitor Design Revealed by Crystal Structures of Imidazoleisoindole Derivatives with IDO1

Peng, Yi-Hui,Ueng, Shau-Hua,Tseng, Chen-Tso,Hung, Ming-Shiu,Song, Jen-Shin,Wu, Jian-Sung,Liao, Fang-Yu,Fan, Yu-Shiou,Wu, Mine-Hsine,Hsiao, Wen-Chi,Hsueh, Ching-Cheng,Lin, Shu-Yu,Cheng, Chia-Yi,Tu, Chih-Hsiang,Lee, Lung-Chun,Cheng, Ming-Fu,Shia, Kak-Shan,Shih, Chuan,Wu, Su-Ying

, p. 282 - 293 (2016)

Indoleamine 2,3-dioxygenase 1 (IDO1), promoting immune escape of tumors, is a therapeutic target for the cancer immunotherapy. A number of IDO1 inhibitors have been identified, but only limited structural biology studies of IDO1 inhibitors are available t

Direct synthesis of pyrroles via a silver-promoted three-component reaction involving unusual imidazole ring opening

Zeng, Jing,Bai, Yaguang,Cai, Shuting,Ma, Jimei,Liu, Xue-Wei

supporting information; experimental part, p. 12855 - 12857 (2012/02/03)

A novel silver-promoted three-component reaction toward the synthesis of multifunctionalized pyrroles has been developed. This reaction involves an unusual imidazole ring decomposition, presumably via 1,5-isomerization and subsequent hydrolysis.

Substituted inmidazoles as bombesin receptor subtype-3 modulators

-

Page/Page column 27-28, (2010/02/17)

Certain novel substituted imidazoles are ligands of the human bombesin receptor and, in particular, are selective ligands of the human bombesin receptor subtype-3 (BRS-3). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of BRS-3, such as obesity, and diabetes.

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