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2-Methyl-6-isobutyrylnaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73652-97-8

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73652-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73652-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,5 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73652-97:
(7*7)+(6*3)+(5*6)+(4*5)+(3*2)+(2*9)+(1*7)=148
148 % 10 = 8
So 73652-97-8 is a valid CAS Registry Number.

73652-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-(6-methylnaphthalen-2-yl)propan-1-one

1.2 Other means of identification

Product number -
Other names isobutyryl-6 methyl-2 naphtalene

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:73652-97-8 SDS

73652-97-8Relevant academic research and scientific papers

Synthesis, structure and pharmacological activity of acyl-2-naphthalene acetic acids and derivatives

Saint Martino Descours,Pacheco,Venco,Yavordios

, p. 5 - 9 (2007/10/02)

Acyl 2-naphthalene acetic derivatives are obtained by a Friedel and Crafts reaction from methyl 2-naphthalene acetate. Low polarity solvents permit selective acylation in the 5 and 8 position, polar solvents in position 6 and 7. The structure of these products is demonstrated by NMR spectra (250 MHz) studies. Unambiguous syntheses of several of them were performed. Acyl 2-naphthalene acetic derivatives show lower anti-inflammatory, analgesic and antipyretic activities in animals than their 1-naphthalene analogs.

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