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472-64-0

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472-64-0 Usage

Description

2,6,6-trimethyl-2-cyclohexene-1-acetaldehyde is a colorless liquid chemical compound with the molecular formula C10H16O. It is characterized by a fruity odor and is commonly used in the fragrance and flavor industry.

Uses

Used in Flavor Industry:
2,6,6-trimethyl-2-cyclohexene-1-acetaldehyde is used as a flavoring agent for its fruity aroma, particularly in the production of artificial fruit flavors.
Used in Perfume Industry:
2,6,6-trimethyl-2-cyclohexene-1-acetaldehyde is used as a scent component in the production of perfumes and other scented products, due to its pleasant odor.
Used in Consumer Goods:
2,6,6-trimethyl-2-cyclohexene-1-acetaldehyde is a popular choice for use in consumer goods, such as air fresheners and cleaning products, because of its relatively low toxicity and appealing scent.

Check Digit Verification of cas no

The CAS Registry Mumber 472-64-0 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 472-64:
(5*4)+(4*7)+(3*2)+(2*6)+(1*4)=70
70 % 10 = 0
So 472-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O/c1-9-5-4-7-11(2,3)10(9)6-8-12/h5,8,10H,4,6-7H2,1-3H3

472-64-0SDS

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-cyclohexenyl)acetaldehyde

1.2 Other means of identification

Product number -
Other names 2,6,6-TRIMETHYL-2-CYCLOHEXEN-1-ACETALDEHYDE

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:472-64-0 SDS

472-64-0Relevant 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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