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N-[(2-hydroxynaphthalen-1-yl)methyl]-N-methylacetamide is a complex organic compound with the molecular formula C12H13NO2. It is characterized by a naphthalene ring with a hydroxyl group at the 2-position, which is connected to a methylene group. This methylene group then links to an acetamide moiety, which consists of a methyl group attached to the nitrogen atom of an amide group. The compound is known for its potential applications in various chemical and pharmaceutical processes, including the synthesis of certain drugs and intermediates. Its structure provides a unique set of properties that can be exploited in different chemical reactions, making it a valuable component in the field of organic chemistry.

7507-65-5

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7507-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7507-65-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7507-65:
(6*7)+(5*5)+(4*0)+(3*7)+(2*6)+(1*5)=105
105 % 10 = 5
So 7507-65-5 is a valid CAS Registry Number.

7507-65-5SDS

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-[(2-hydroxynaphthalen-1-yl)methyl]-N-methylacetamide

1.2 Other means of identification

Product number -
Other names N-(2-Hydroxy-[1]naphthylmethyl)-N-methyl-acetamid

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 -
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More Details:7507-65-5 SDS

7507-65-5Relevant academic research and scientific papers

N-Alkylamidomethylation at Electron-rich Carbons in the 1,3,5-Trialkylhexahydro-1,3,5-triazine-Acetyl Chloride System

Ikeda, Kiyoshi,Morimoto, Toshiaki,Sekiya, Minoru

, p. 1178 - 1182 (2007/10/02)

A new N-alkylamidomethylation reaction at electron-rich carbons has been developed using 1,3,5-trialkylhexahydro-1,3,5-triazine in the presence of acetyl chloride.This reaction was carried out not only with aromatics such as phenols, alkoxybenzenes and aromatic amines, but also olefins such as styrene and vinyl ethers. Keywords---N-alkylamidomethylation; electrophilic substitution; 1,3,5-trialkylhexahydro-1,3,5-triazines; acetyl chloride; aromatics; styrene; vinyl ethers

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