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2-(1-cyclohexylpropan-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.

41625-76-7

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41625-76-7 Usage

Chemical class

Oxazines
Heterocyclic compounds containing both nitrogen and oxygen atoms in their structure.

Molecular structure

2-(1-cyclohexylpropan-2-yl)-4,4,6-trimethyl-5,6-dihydro-4H-1,3-oxazine
A specific arrangement of atoms in the compound, including cyclohexyl and propan-2-yl substituents.

Physical state

Colorless liquid at room temperature
The compound's appearance and state under standard conditions.

Usage

Building block in the synthesis of other organic compounds
The compound serves as an intermediate in creating more complex organic molecules.

Industries

Pharmaceutical and pesticide
The compound is utilized in these industries due to its biological activity and potential applications.

Biological activity

Known for its effects on living organisms
The compound exhibits properties that allow it to interact with biological systems, making it a valuable research and development target.

Check Digit Verification of cas no

The CAS Registry Mumber 41625-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,2 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41625-76:
(7*4)+(6*1)+(5*6)+(4*2)+(3*5)+(2*7)+(1*6)=107
107 % 10 = 7
So 41625-76-7 is a valid CAS Registry Number.

41625-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-cyclohexylpropan-2-yl)-4,4,6-trimethyl-5,6-dihydro-1,3-oxazine

1.2 Other means of identification

Product number -
Other names 2-(1-cyclohexyl-2-propyl)-4,4,6-trimethyl-5,6-dihydro-1,3-4H-oxazine

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:41625-76-7 SDS

41625-76-7Downstream Products

41625-76-7Relevant 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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