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1-methyl-1-(m-tolyl)ethyl acetate is an organic compound with the molecular formula C12H16O2. It is a colorless liquid with a fruity, floral odor and is commonly used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions. This ester is synthesized by the esterification of 1-methyl-1-(m-tolyl)ethanol with acetic acid, resulting in a compound that possesses a pleasant, sweet scent. Due to its low toxicity and excellent stability, 1-methyl-1-(m-tolyl)ethyl acetate is widely employed in the fragrance industry to enhance the aroma of various products.

7323-70-8

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7323-70-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7323-70-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7323-70:
(6*7)+(5*3)+(4*2)+(3*3)+(2*7)+(1*0)=88
88 % 10 = 8
So 7323-70-8 is a valid CAS Registry Number.

7323-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-1-(m-tolyl)ethyl acetate

1.2 Other means of identification

Product number -
Other names m-cymenyl acetate

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:7323-70-8 SDS

7323-70-8Downstream Products

7323-70-8Relevant academic research and scientific papers

Oxidative Decarboxylation of Some Bicyclohept-3-ene-1-carboxylic Acids

Galloway, Neil,Dent, Barry R.,Halton, Brian

, p. 593 - 599 (2007/10/02)

Treatment of the bicyclohept-3-ene-1-carboxylic acids (8d-f) with lead tetraacetate results in oxidative decarboxylation and formation of the 1-aryl-1-methylethyl acetates (12a-c).

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