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Cyclododecylethylether, also known as 1-(2-ethoxyethyl)cyclododecane, is a cyclic ether compound with a molecular formula of C16H32O. It features a cyclododecane ring (a twelve-carbon cyclic structure) with an ethyl ether group attached to one of its carbon atoms. This ether group consists of an oxygen atom bonded to two carbon atoms, one of which is part of the cyclododecane ring, and the other is an ethyl group. Cyclododecylethylether is a colorless liquid with a low melting point and is insoluble in water. It is used in various applications, including as a solvent, a chemical intermediate, and in the synthesis of other organic compounds. Due to its unique structure, it can form strong intermolecular interactions, which can influence its physical and chemical properties.

2986-53-0

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2986-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2986-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2986-53:
(6*2)+(5*9)+(4*8)+(3*6)+(2*5)+(1*3)=120
120 % 10 = 0
So 2986-53-0 is a valid CAS Registry Number.

2986-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethoxycyclododecane

1.2 Other means of identification

Product number -
Other names Cyclododecane,ethoxy

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:2986-53-0 SDS

2986-53-0Downstream Products

2986-53-0Relevant academic research and scientific papers

A new method of synthesis of cyclododecyl ethers

Balbolov,Mitkova

, p. 88 - 91 (2007/10/03)

Cyclododecyl ethers were synthesized by substitutive alkoxylation of isomeric acetoxycyclododeca-2,6,10-trienes with aliphatic alcohols in the presence of Pd[PPh3]4, followed by hydrogenation of the double bonds. The kinetics of the substitutive alkoxylation of isomeric cyclododecatrien-1-yl acetate with 2-methoxyethanol at 358°C were studied.

Odor-structure relationships using fluorine as a probe

Michel, Dominique,Schlosser, Manfred

, p. 4253 - 4260 (2007/10/03)

Eight ethers, nine esters and one ketone were submitted to a systematic structural variation by replacing a hydrogen atom in the vicinity of the oxofunction by fluorine and methyl. As long as steric factors dominate, a fluorine substituent alters the olfactory properties of the parent compound much less than a methyl substituent does. However, if it occupies a position adjacent to a carbonyl group, the halogen may more profoundly affect the odor perception, presumably as a consequence of conformational changes. (C) 2000 Elsevier Science Ltd.

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