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CAS

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472-67-3

2-Cyclohexene-1-acetic acid, 2,6,6-trimethyl- is an organic compound with the chemical formula C11H18O2. It is a derivative of cyclohexane, featuring a cyclohexene ring with a carboxylic acid group attached to the 1-position and a methyl group at the 2-position. Additionally, there are two methyl groups at the 6-position, which contribute to its molecular structure. 2-Cyclohexene-1-acetic acid, 2,6,6-trimethyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. Its unique structure and properties make it an important molecule in the field of organic chemistry.

472-67-3

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472-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 472-67-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 472-67:
(5*4)+(4*7)+(3*2)+(2*6)+(1*7)=73
73 % 10 = 3
So 472-67-3 is a valid CAS Registry Number.

472-67-3SDS

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 (2,6,6-Trimethyl-2-cyclohexen-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names cyclogeranyl bromide

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:472-67-3 SDS

472-67-3Downstream Products

472-67-3Relevant articles and documents

Limonoid model insect antifeedants. A stereoselective synthesis of azadiradione C, D, and E fragments through intramolecular diazo ketone cyclization

Fernandez Mateos,Lopez Barba

, p. 3580 - 3585 (2007/10/02)

A stereoselective synthesis of model compound 18 of the insect antifeedant azadiradione has been accomplished starting from α-cyclocitral in 12 steps in 15% overall yield. The strategy for the synthesis is based on an intramolecular cyclopropanation of a diazo ketone and subsequent selective cleavage of a cyclopropyl ketone. Reactivity differences in the cleavage of the key cyclopropyl ketone 13 and its homolog 12 lacking the furyl ring are explored.

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