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N-{[2-(3-chloro-4-methoxyphenyl)-1,3-benzoxazol-5-yl]carbamothioyl}-4-methoxybenzamide is a complex organic compound with the molecular formula C21H15ClN2O4S. It is characterized by a benzoxazole ring, which is fused with a benzene ring, and a carbamothioyl group attached to the benzene ring. The compound also features a 3-chloro-4-methoxyphenyl group and a 4-methoxybenzamide group, which contribute to its overall structure and properties. This chemical is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique molecular structure and reactivity.

6405-72-7

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6405-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6405-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6405-72:
(6*6)+(5*4)+(4*0)+(3*5)+(2*7)+(1*2)=87
87 % 10 = 7
So 6405-72-7 is a valid CAS Registry Number.

6405-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[2-(3-chloro-4-methoxyphenyl)-1,3-benzoxazol-5-yl]carbamothioyl]-4-methoxybenzamide

1.2 Other means of identification

Product number -
Other names Phenylglyoxylsaeure-cholesterylester

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:6405-72-7 SDS

6405-72-7Downstream Products

6405-72-7Relevant academic research and scientific papers

Heterogeneous Esterification from α-Hydroxy Ketone and Alcohols through a Tandem Oxidation Process over a Hydrotalcite-Supported Bimetallic Catalyst

Meng, Xu,Bi, Xiuru,Chen, Gexin,Chen, Baohua,Zhao, Peiqing

, p. 1716 - 1722 (2018/10/25)

Heterogeneous aerobic oxidative esterification between α-hydroxy ketone and alcohols catalyzed by a hydrotalcite-supported bimetallic catalyst (CuMn/HT) using O2 as a green oxidant was achieved. Recyclable CuMn/HT exhibits high catalytic activity due to increased content of oxygen vacancies and a newly generated CuMn2O4 crystal phase. This clean esterification proceeds through a tandem oxidation process in the absence of any additives and ligands and affords α-keto esters in good to excellent yields. Moreover, the catalytic system tolerates complicated bioactive molecules as raw materials and can be performed on a multigram scale.

Cu-catalyzed aerobic oxidative esterification of acetophenones with alcohols to ?±-ketoesters

Xu, Xuezhao,Ding, Wen,Lin, Yuanguang,Song, Qiuling

supporting information, p. 516 - 519 (2015/03/03)

Copper-catalyzed aerobic oxidative esterification of acetophenones with alcohols using molecular oxygen has been developed to form a broad range of ?±-ketoesters in good yields. In addition to reporting scope and limitations of our new method, mechanism studies are reported that reveal that the carbonyl oxygen in the ester mainly originated from dioxygen.

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