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92437-06-4

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92437-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92437-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,3 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92437-06:
(7*9)+(6*2)+(5*4)+(4*3)+(3*7)+(2*0)+(1*6)=134
134 % 10 = 4
So 92437-06-4 is a valid CAS Registry Number.

92437-06-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-phenylphenyl)-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-BIPHENYL-2-YL-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:92437-06-4 SDS

92437-06-4Downstream Products

92437-06-4Relevant articles and documents

Palladium-Catalyzed Direct Monoarylation of Aryl C?H Bonds with Iodoarenes

Su, Li,Guo, Dong-Dong,Li, Bin,Guo, Shi-Huan,Pan, Gao-Fei,Gao, Ya-Ru,Wang, Yong-Qiang

, p. 2001 - 2008 (2017/06/13)

The transition-metal-catalyzed direct arylation of nonactivated aryl C?H bonds with iodoarenes has emerged as an important method for the construction of biaryls. Generally, the direct arylation reaction proceeds in the presence of stoichiometric Ag additives; moreover, the diarylation product is often unavoidable if there are two identical aromatic C?H bonds in the substrate. Herein we disclose an efficient Pd(OAc)2/trifluoroacetic acid/O2 catalytic system that promotes direct arylation reactions of a variety of aromatic C?H bonds with diverse iodoarenes under Ag-free conditions. The coupling reaction possesses a complete monoarylation selectivity. This approach provides a straightforward, facile, and economical route to biaryls.

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