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2,7-dimethylcycloheptanone is a cyclic ketone with the molecular formula C9H16O. It is an organic compound characterized by a seven-membered carbon ring, with two methyl groups attached at the 2nd and 7th positions. This ketone is known for its unique aroma and is often used in the fragrance industry to create floral and fruity scents. It is also employed as a flavoring agent in food and beverages, imparting a sweet, fruity taste. The compound is synthesized through various chemical reactions and is an important intermediate in the production of certain pharmaceuticals and agrochemicals. Due to its chemical structure, 2,7-dimethylcycloheptanone exhibits specific properties that make it a versatile compound in the fields of chemistry, biology, and material science.

7272-19-7

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7272-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7272-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7272-19:
(6*7)+(5*2)+(4*7)+(3*2)+(2*1)+(1*9)=97
97 % 10 = 7
So 7272-19-7 is a valid CAS Registry Number.

7272-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dimethylcycloheptanone

1.2 Other means of identification

Product number -
Other names 2,7-Dimethylcycloheptanon

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

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More Details:7272-19-7 SDS

7272-19-7Downstream Products

7272-19-7Relevant academic research and scientific papers

Selective homologation of ketones and aldehydes with diazoalkanes promoted by organoaluminum reagents

Maruoka,Concepcion,Yamamoto

, p. 1283 - 1290 (2007/10/02)

Organoaluminum-promoted single homologation or ring expansion of ketones and aldehydes with diazoalkanes has been described, and among various organoaluminium reagents, exceptionally bulky methylaluminum bis(2,6-di-tert-butyl-4-methylphenoxide) (MAD) is found to be highly effective for the selective homologation of various ketones and aldehydes.

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