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2-(2,6-Dimethyl-5-heptenyl)oxazolidine-3-ethanol is a complex organic compound with the molecular formula C12H23NO2. It is a colorless liquid with a molecular weight of 213.32 g/mol. This chemical is characterized by the presence of an oxazolidine ring, which is a five-membered heterocyclic ring containing two oxygen atoms and one nitrogen atom. The compound also features a 2,6-dimethyl-5-heptenyl group, which is an alkenyl chain with two methyl groups at the 2nd and 6th carbon positions. The 3-ethanol group indicates the presence of an ethanol moiety attached to the 3rd carbon of the oxazolidine ring. 2-(2,6-Dimethyl-5-heptenyl)oxazolidine-3-ethanol is primarily used as a fragrance ingredient in various consumer products, such as perfumes, cosmetics, and personal care items, due to its pleasant, floral scent. It is also known for its antimicrobial properties, making it a potential candidate for use in pharmaceutical and industrial applications.

42822-96-8

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42822-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42822-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,2 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42822-96:
(7*4)+(6*2)+(5*8)+(4*2)+(3*2)+(2*9)+(1*6)=118
118 % 10 = 8
So 42822-96-8 is a valid CAS Registry Number.

42822-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-dimethyl-5-heptenyl)-3-oxazolidineethanol

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:42822-96-8 SDS

42822-96-8Relevant academic research and scientific papers

Preparation method of citronellal hydrate

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Paragraph 0065; 0067; 0068; 0076; 0084; 0092; 0100, (2018/04/03)

The invention relates to a preparation method of citronellal hydrate. The method comprises the steps of citronellal oxazolidine derivative preparation, solid acid catalytic reaction, aftertreatment and the like. The purity of a citronellal hydrate product prepared by using the method provided by the invention reaches 95% or above. The method provided by the invention has the characteristics that asolid acidification catalyst is easily separated from a reactant, can be repeatedly used and cannot corrode a reactor, catalytic public hazards are reduced, and the wastewater amount is greatly reduced. By using the method provided by the invention, an environment-friendly synthesis process route is achieved.

PREPARATION OF DERIVATIVES OF CITRONELLAL

Koertvelyessy, Gyula

, p. 347 - 354 (2007/10/02)

The hydrogenation of citronellal and citral, if not separated from ethereal oils, leads regioselectively to dihydrocitronellal and citronellal, respectively.The reaction of citral with (+)-ephedrin or L-aspartic acid, followed by hydrogenation and deblocking the aldehyde function, yields optically active citronellal.Reacting the aldehyde function of citronellal with diethanolamine, piperidine or morpholine, the alcohol addition to the 6,7-double bond results in 7-alkoxy substituted citronellals with acceptable yield.The formation of 7-hydroxy-6,7-dihydrocitronellal during this reaction has been proved and the effect of reaction parameters on the yield have been discussed.

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