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2-(4,4-dimethylpentan-2-yl)-4,4,6-trimethyl-5,6-dihydro-4H-1,3-oxazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39575-86-5

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39575-86-5 Usage

Class of compound

Organic compound, specifically an oxazine.

Physical state

Colorless liquid.

Odor

Faint.

Primary use

Solvent in various industrial processes.

Molecular structure

Contains a six-membered ring with oxygen and nitrogen atoms, and multiple methyl groups.

Stability

Contributed by multiple methyl groups.

Solubility

Contributed by multiple methyl groups.

Toxicity

Not known to have any significant toxic effects on human health or the environment.

Safety

Generally considered to be safe for use in regulated applications.

Check Digit Verification of cas no

The CAS Registry Mumber 39575-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,7 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39575-86:
(7*3)+(6*9)+(5*5)+(4*7)+(3*5)+(2*8)+(1*6)=165
165 % 10 = 5
So 39575-86-5 is a valid CAS Registry Number.

39575-86-5SDS

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-(4,4-dimethylpentan-2-yl)-4,4,6-trimethyl-5,6-dihydro-1,3-oxazine

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:39575-86-5 SDS

39575-86-5Downstream Products

39575-86-5Relevant academic research and scientific papers

Synthesis of aldehydes and products of such synthesis

-

, (2008/06/13)

The disclosure describes the production of complex aliphatic, unsaturated and cycloalkane aldehydes utilizing heterocyclic ring compounds, such as oxazines, particularly dihydro-1,3-oxazines. The oxazines are treated with an alkali metal-alkane compound, such as butyl lithium in the presence of an organic solvent at subzero temperature to form an anion of the oxazine. This anion is then alkylated in the anhydrous reaction mixture by introduction of a suitable halide, epoxide or ketone while still at a subzero temperature and mixture is permitted to warm up to room temperature, following which the reaction mixture is acidified, as with hydrochloric acid to pH 2 to 3, extracted and then made basic, as with caustic alkali with cooling. The reaction mixture is then extracted, as with ether, to produce after evaporation the alkylated dihydro-1,3-oxazine. The alkylated dihydro-1,3-oxazine is then reacted with an alkali metal or sodium borohydride or borodeuteride or borotritide, with cooling to subzero temperatures at about a neutral pH and then transferred into a basic aqueous environment following extraction of the aqueous layer with an organic solvent, such as ether, to give a tetrahydro-1,3-oxazine. This compound may then be converted to the aldehyde desired by steam distillation or by hydrolysis in the presence of a dilute or weak acid, such as hydrochloric or oxalic acid. The aldehydes may then be extracted. These aldehydes are useful as components or intermediates in flavoring or perfumes, in insect attractants and repellants, and in pharmaceuticals.

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