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2-Acetylcyclododecanone is a chemical compound with the molecular formula C15H26O. It is a cyclic ketone, characterized by a twelve-membered carbon ring with a ketone group (C=O) attached to the second carbon atom and an acetyl group (CH3CO-) attached to the same carbon. 2-acetylcyclododecanone is known for its strong, musky odor and is commonly used as a fragrance ingredient in perfumes and cosmetics due to its long-lasting scent. It is also found in nature, particularly in the secretions of certain animals, and can be synthesized for commercial use. The compound's unique structure contributes to its distinctive smell, making it a valuable component in the creation of various scent profiles.

1686-92-6

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1686-92-6 Usage

Type

Cyclic ketone derivative of cyclododecane

Common uses

Fragrance, flavor, pharmaceutical industries

Odor

Pleasant, musk-like

Function

Fragrance enhancer
Building block in organic compound synthesis

Pharmacological activities

Antitumor, antioxidant properties

Stability

Relatively stable

Toxicity

Non-toxic

Check Digit Verification of cas no

The CAS Registry Mumber 1686-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1686-92:
(6*1)+(5*6)+(4*8)+(3*6)+(2*9)+(1*2)=106
106 % 10 = 6
So 1686-92-6 is a valid CAS Registry Number.

1686-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetylcyclododecanone

1.2 Other means of identification

Product number -
Other names -

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:1686-92-6 SDS

1686-92-6Upstream product

1686-92-6Relevant academic research and scientific papers

Synthesis of β-oxo carbonyl and thiocarbonyl compounds via basic sulfur abstraction

Silva, Saúl,Maycock, Christopher D.

, (2019/09/10)

Sulfur abstraction from suitable thioesters represents a mild method for the formation of carbon-carbon bonds and the formation of 1,3-dicarbonyl compounds. A study of the scope and limitations of this reaction for the synthesis of these or mixed 1,3-carbonyl/thiocarbonyl compounds by a base promoted sulfur abstraction rearrangement is described. These reactions were typically very clean and the products were obtained in good yield (65–95%) in just 30 min. This method is particularly efficient for the introduction of thiocarbonyl containing groups. Thus, it constitutes a synthetic strategy for the generation of a new carbon-carbon bond and the regioselective preparation of mixed β-dicarbonyl compounds.

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