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Cyclododecyl isobutyl ether is a complex organic compound with the molecular formula C18H36O. It is a cyclic ether, characterized by a twelve-membered ring (cyclododecane) with an isobutyl group attached to one of its carbon atoms. This ether is known for its unique structure and properties, which can be utilized in various chemical reactions and applications. It is typically synthesized through the reaction of cyclododecanol with isobutyl bromide in the presence of a base, such as potassium hydroxide. Cyclododecyl isobutyl ether is a colorless liquid with a low boiling point and is insoluble in water. Due to its specific chemical structure, it can be used as a solvent, a reagent in organic synthesis, or as a component in the production of specialty chemicals. Its stability and reactivity make it a valuable compound in the field of organic chemistry.

2986-50-7

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2986-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2986-50-7 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 2986-50:
(6*2)+(5*9)+(4*8)+(3*6)+(2*5)+(1*0)=117
117 % 10 = 7
So 2986-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H32O/c1-15(2)14-17-16-12-10-8-6-4-3-5-7-9-11-13-16/h15-16H,3-14H2,1-2H3

2986-50-7SDS

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 2-methylpropoxycyclododecane

1.2 Other means of identification

Product number -
Other names cyclododecyl isobutyl ether

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:2986-50-7 SDS

2986-50-7Downstream Products

2986-50-7Relevant academic research and scientific papers

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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