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207926-35-0

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207926-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207926-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,2 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 207926-35:
(8*2)+(7*0)+(6*7)+(5*9)+(4*2)+(3*6)+(2*3)+(1*5)=140
140 % 10 = 0
So 207926-35-0 is a valid CAS Registry Number.

207926-35-0SDS

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 N-(5-bromopyridin-2-yl)-2,2,2-trifluoroacetamide

1.2 Other means of identification

Product number -
Other names N-(5-bromopyrid-2-yl)-2,2,2-trifluoro-acetamide

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:207926-35-0 SDS

207926-35-0Downstream Products

207926-35-0Relevant articles and documents

A Chemoselective N-Arylation Reaction of 2-Aminopyridine Derivatives with Arynes

Cheng, Bin,Wei, Jian,Zu, Bing,Zhao, Jianfei,Wang, Taimin,Duan, Xiaoguang,Wang, Renqi,Li, Yun,Zhai, Hongbin

, p. 9410 - 9417 (2017)

A chemoselective N-arylation reaction of 2-aminopyridine derivatives with arynes in good to excellent yields has been described. The N-arylation products could be further applied to the facile construction of benzoisoquinuclidines and isoquinuclidines as

Synthesis of Functionalized 3-Pyridyl Methyl Ketones

Wright,Hageman,McClure

, p. 717 - 723 (2007/10/03)

A synthesis of 3-pyridyl methyl ketones is described that employs a palladium-catalyzed olefination of 3-bromopyridines with butyl vinyl ether followed by acid hydrolysis of the intermediate pyridyl vinyl ether in situ. This method has been applied to bromoquinoline substrates as well. The reaction is compatible with a variety of functional groups.

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