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7-Octen-2-one is a colorless to pale yellow liquid with a strong mushroom-like odor. It is an organic compound with the chemical formula C8H14O and is classified as an aliphatic ketone. 7-Octen-2-one is widely used in the food and fragrance industry as a flavoring agent and a fragrance ingredient, providing a characteristic earthy, mushroom-like aroma. It is also found in various natural sources, such as truffles and some types of mushrooms. In the laboratory, 7-octen-2-one can be synthesized through various methods, including the oxidation of 1-octen-3-ol or the condensation of acetone with heptanal. Due to its unique properties, it plays a significant role in enhancing the sensory experience of various products.

3664-60-6

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3664-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3664-60-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3664-60:
(6*3)+(5*6)+(4*6)+(3*4)+(2*6)+(1*0)=96
96 % 10 = 6
So 3664-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O/c1-3-4-5-6-7-8(2)9/h3H,1,4-7H2,2H3

3664-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-octen-2-one

1.2 Other means of identification

Product number -
Other names oct-7-en-2-one

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:3664-60-6 SDS

3664-60-6Relevant academic research and scientific papers

Liquid-phase isomerization of saturated and unsaturated epoxides

Mel'nik,Khvatova,Moskvichev,Srednev,Egorova

, p. 167 - 169 (2007/10/03)

The liquid-phase isomerization of a variety of epoxides was studied using a complex catalyst system based on magnesium bromide and dimethylformamide. The data obtained elucidate the mechanism of the liquid-phase isomerization and show the range of oxygen-containing compounds which can be prepared through this reaction.

Clemmensen Reduction. XI. Fragmentation Reactions of Some 3-Acetylcycloalkanones

Bailey, Karen E.,Davis, Brian R.

, p. 1827 - 1834 (2007/10/03)

Clemmensen reduction of a series of 3-acetylcycloalkanones yields, as the major product, an acyclic unsaturated ketone, the product of fragmentation.Some normal carbonyl-methylene reduction also occurs.A mechanistic rationale for the fragmentation is advanced.

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