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Acetamide, N-(4-chlorophenyl)-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61667-88-7

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61667-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61667-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,6 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61667-88:
(7*6)+(6*1)+(5*6)+(4*6)+(3*7)+(2*8)+(1*8)=147
147 % 10 = 7
So 61667-88-7 is a valid CAS Registry Number.

61667-88-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-N-(4-chlorophenyl)acetamide

1.2 Other means of identification

Product number -
Other names N-Benzyl-p-chloracetanilid

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:61667-88-7 SDS

61667-88-7Downstream Products

61667-88-7Relevant academic research and scientific papers

A new method for the synthesis of amides from imines

Ghaffarzadeh, Mohammad,Joghan, Somaye Shahrivari,Faraji, Fereshteh

experimental part, p. 203 - 206 (2012/03/07)

An efficient and straightforward method for the synthesis of amides by the reaction of imines and anhydrides in the presence of Et3SiH/Zn is reported. Mild reaction conditions, good yields of products, short reaction times, and operational simplicity are advantages of this procedure.

Synthesis of amides from imines using Et3SiH/Zn system

Ghaffarzadeh, Mohammad,Heidarifard, Somaye,Faraji, Fereshteh,Joghan, Somaye Shahrivari

experimental part, p. 103 - 107 (2012/05/05)

A simple and efficient approach for the synthesis of amides by the reaction of imines and acyl chlorides in the presence of Et3SiH/Zn system in THF at ambient temperature is reported. Mild reaction conditions, good yields of products, short reaction time and operational simplicity are the advantages of this procedure. Copyright

Bioorganic Studies: Part IV - Reductive N-Acylation of Imines Using 3,5-Dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine as NADH Model

Singh, Serjinder,Sharma, Vijay K.

, p. 1087 - 1088 (2007/10/02)

A one-step reductive acetylation of imines (II) using 3,5-dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine (I) as NADH model is reported.The N-acetyliminium intermediates are reduced in situ by I to give N-acetylamines (IV).Reduction of species which stabili

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