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7461-38-3

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7461-38-3 Usage

General Description

4-Chloro-N,N-diethylbenzamide, 97% is a chemical compound with the formula C11H14ClNO. Its systematic name is 4-Chloro-N,N-diethylbenzamide. This specific variation indicates that it comes with a purity factor of 97%, meaning that the majority of the substance is comprised of this particular compound. It's commonly used in a wide range of chemical reactions due to its structure and chemical properties. Its molecular weight is 213.69 g/mol. The compound is hazardous and may cause eye, skin, and respiratory irritation on exposure, and thus should be handled with the correct safety precautions. Its precise uses largely depend on the context in which it is being applied, often in specialized industrial or laboratory settings.

Check Digit Verification of cas no

The CAS Registry Mumber 7461-38-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7461-38:
(6*7)+(5*4)+(4*6)+(3*1)+(2*3)+(1*8)=103
103 % 10 = 3
So 7461-38-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H14ClNO/c1-3-13(4-2)11(14)9-5-7-10(12)8-6-9/h5-8H,3-4H2,1-2H3

7461-38-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H59284)  4-Chloro-N,N-diethylbenzamide, 97%   

  • 7461-38-3

  • 250mg

  • 1260.0CNY

  • Detail
  • Alfa Aesar

  • (H59284)  4-Chloro-N,N-diethylbenzamide, 97%   

  • 7461-38-3

  • 1g

  • 4032.0CNY

  • Detail

7461-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-N,N-diethylbenzamide

1.2 Other means of identification

Product number -
Other names 4-chloro-N,N-diethyl-benzamide

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:7461-38-3 SDS

7461-38-3Relevant articles and documents

An efficient approach to 3-bromo-6-chloro-phenanthrene-9,10-dione

Limanto, John,Domer, Benjamin T.,Hartner, Frederick W.,Tan, Lushi

, p. 1269 - 1272 (2008)

A practical and efficient synthesis of 3-bromo-6-chloro-phenanthrene-9,10- dione was developed and demonstrated on a large scale. The synthetic approach involves six chemical steps and two isolations in 73% overall yield. The key transformations feature a

One-Pot Synthesis of Tertiary Amides from Organic Trichlorides through Oxygen Atom Incorporation from Air by Convergent Paired Electrolysis

Luo, Zhongli,Imamura, Kenji,Shiota, Yoshihito,Yoshizawa, Kazunari,Hisaeda, Yoshio,Shimakoshi, Hisashi

, p. 5983 - 5990 (2021/05/04)

A convergent paired electrolysis catalyzed by a B12 complex for the one-pot synthesis of a tertiary amide from organic trichlorides (R-CCl3) has been developed. Various readily available organic trichlorides, such as benzotrichloride and its derivatives, chloroform, dichlorodiphenyltrichloroethane (DDT), trichloro-2,2,2-trifluoroethane (CFC-113a), and trichloroacetonitrile (CNCCl3), were converted to amides in the presence of tertiary amines through oxygen incorporation from air at room temperature. The amide formation mechanism in the paired electrolysis, which was mediated by a cobalt complex, was proposed.

Visible Light-Driven Efficient Synthesis of Amides from Alcohols using Cu?N?TiO2 Heterogeneous Photocatalyst

Singha, Krishnadipti,Ghosh, Subhash Chandra,Panda, Asit Baran

supporting information, p. 657 - 662 (2021/02/02)

Amides were synthesized from alcohols and amines in high yields using an in situ generated active ester of N-hydroxyimide with our developed Cu?N?TiO2 catalyst at room temperature using oxygen as a sole oxidant under visible light. The catalyst can be easily prepared, robust, and recycled four times without a considerable change in catalytic activity. This developed protocol applies to a wide substrate scope and has good functional group tolerance. The application of this amidation reaction has been successfully demonstrated for the synthesis of moclobemide, an antidepressant drug, and an analog of the itopride drug on a gram scale.

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