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620-81-5

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620-81-5 Usage

Chemical Properties

WHITE TO OFF-WHITE FLAKY POWDER

Uses

Oxanilide is useful in the synthesis of metal complexs as it can be used as a bidentate ligand.

Check Digit Verification of cas no

The CAS Registry Mumber 620-81-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 620-81:
(5*6)+(4*2)+(3*0)+(2*8)+(1*1)=55
55 % 10 = 5
So 620-81-5 is a valid CAS Registry Number.

620-81-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (L07369)  Oxanilide, 97%   

  • 620-81-5

  • 5g

  • 116.0CNY

  • Detail
  • Alfa Aesar

  • (L07369)  Oxanilide, 97%   

  • 620-81-5

  • 25g

  • 471.0CNY

  • Detail
  • Alfa Aesar

  • (L07369)  Oxanilide, 97%   

  • 620-81-5

  • 5g

  • 116.0CNY

  • Detail
  • Alfa Aesar

  • (L07369)  Oxanilide, 97%   

  • 620-81-5

  • 25g

  • 471.0CNY

  • Detail
  • Alfa Aesar

  • (L07369)  Oxanilide, 97%   

  • 620-81-5

  • 5g

  • 116.0CNY

  • Detail
  • Alfa Aesar

  • (L07369)  Oxanilide, 97%   

  • 620-81-5

  • 25g

  • 471.0CNY

  • Detail
  • Alfa Aesar

  • (L07369)  Oxanilide, 97%   

  • 620-81-5

  • 5g

  • 116.0CNY

  • Detail
  • Alfa Aesar

  • (L07369)  Oxanilide, 97%   

  • 620-81-5

  • 25g

  • 471.0CNY

  • Detail

620-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-diphenyloxamide

1.2 Other means of identification

Product number -
Other names Oxamide,N,N'-diphenyl

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:620-81-5 SDS

620-81-5Relevant articles and documents

Copper-Catalyzed Ullmann-Type Coupling and Decarboxylation Cascade of Arylhalides with Malonates to Access α-Aryl Esters

Chen, Fen-Er,Chen, Tao,Cheng, Fei,Huang, Yin-Qiu,Li, Jia-Wei,Xiao, Xiao,Zhou, Chen

supporting information, (2022/01/04)

We have developed a high-efficiency and practical Cu-catalyzed cross-coupling to directly construct versatile α-aryl-esters by utilizing readily available aryl bromides (or chlorides) and malonates. These gram-scale approaches occur with turnovers of up to 1560 and are smoothly conducted by the usage of a low catalyst loading, a new available ligand, and a green solvent. A variety of functional groups are tolerated, and the application occurs with α-aryl-esters to access nonsteroidal anti-inflammatory drugs (NSAIDs) on the gram scale.

Visible-light-induced direct construction of amide bond from carboxylic acids with amines in aqueous solution

Wang, Jin,Hou, Huiqing,Hu, Yongzhi,Lin, Jin,Wu, Min,Zheng, Zhiqiang,Xu, Xiuzhi

supporting information, (2021/02/09)

A novel visible-light-promoted N-acylation for the synthesis of amides from easily available carboxylic acids with amines in the presence of I2 within 2.5 h in aqueous solution has been developed. Using sunlight as the visible light source greatly reduces the cost of experiments and produces almost no toxic effects. Hence, this study provides an alternative catalytic system for the construction of a wide range of amides with readily available materials. Moreover, the strategy was successfully applied in the preparation of N-(3-(2,6-dimethoxyphenoxy)-7-nitroquinoxalin-2-yl)benzohydrazide, which displayed a signification anti-proliferation effect on A549, MCF-7 and HCT116 cell lines.

Preparation method of oxamide

-

Paragraph 0062; 0063; 0070; 0071; 0088, (2019/08/03)

The invention provides a preparation method of oxamide. The preparation method comprises the following steps: an intermediate oxamide derivative is prepared from CO, O2 and amine compounds as raw materials by oxidation and carbonylation under the action of a catalyst 1, and then, oxamide is prepared through aminolysis of the oxamide derivative under the action of a catalyst 2. A novel method is used for coproducing oxamide and the oxamide derivative, and the problems that oxalate synthesis materials are poisonous, catalyst efficiency is low and the like in the original technology for synthesizing oxamide through aminolysis of oxalate are solved. Besides, the technologically synthesized oxamide derivative has good substrate applicability and can be applied to fields of medicine, pesticides,synthetic ligands, food additives and the like.

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