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3663-30-7

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3663-30-7 Usage

General Description

N-(4-dodecylphenyl)acetamide is a chemical compound that belongs to the class of organic compounds known as fatty acid amides. It is derived from the condensation reaction between 4-dodecylphenol and acetic acid. N-(4-dodecylphenyl)acetamide is used as an intermediate in the production of various other chemicals and materials, and it is commonly employed as a surfactant and corrosion inhibitor. Its long hydrocarbon tail makes it suitable for use in lubricants, and it also has potential applications in pharmaceuticals and as a stabilizer in plastics. N-(4-dodecylphenyl)acetamide is considered to be biodegradable and of low toxicity, making it a relatively environmentally friendly compound.

Check Digit Verification of cas no

The CAS Registry Mumber 3663-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3663-30:
(6*3)+(5*6)+(4*6)+(3*3)+(2*3)+(1*0)=87
87 % 10 = 7
So 3663-30-7 is a valid CAS Registry Number.

3663-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-dodecylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names n-dodecyl-4 acetanilide

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:3663-30-7 SDS

3663-30-7Relevant articles and documents

Visible-Light-Induced Nickel-Catalyzed Cross-Coupling with Alkylzirconocenes from Unactivated Alkenes

Bai, Songlin,Gao, Yadong,Jiang, Chao,Liu, Xiaolei,Qi, Xiangbing,Wang, Jing,Wu, Qingcui,Yang, Chao

supporting information, p. 675 - 688 (2020/03/11)

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4-higher alkyl-2-nitro-2'-hydroxy-3',5'-di-higher alkyl (or cumyl)-azobenzenes

-

, (2008/06/13)

4-Higher alkyl-2-nitro-2'-hydroxy-3',5'-di-higher alkyl (or cumyl)-azobenzenes are made by coupling the corresponding diazotized 4-higher alkyl-o-nitroaniline with the corresponding substituted phenol. These azobenzene intermediates are used to prepare the corresponding 2H-benzotriazole UV absorber stabilizers substituted on the 5-position of the benzo ring by a higher alkyl group, preferably tert-octyl or n-dodecyl.

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