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4,4,6-Trimethyl-1,3-oxazinan-2-one, also known as N,N-dimethyl-4,4,6-(trimethyl-1,3-oxazinane-2-one, is a chemical compound with the molecular formula C9H15NO2. It is a lactam, which is a type of organic compound that contains a cyclic amide group. 4,4,6-trimethyl-1,3-oxazinan-2-one has a molecular weight of 169.22 g/mol and appears as a clear, colorless liquid at room temperature. It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds, serving as a building block in the production of various fine chemicals and as an important reagent in organic chemistry research.

27830-77-9

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27830-77-9 Usage

Uses

Used in Pharmaceutical Industry:
4,4,6-Trimethyl-1,3-oxazinan-2-one is used as an intermediate in the synthesis of pharmaceuticals for its ability to form complex molecular structures that can be utilized in the development of new drugs.
Used in Organic Chemistry Research:
4,4,6-trimethyl-1,3-oxazinan-2-one is used as a building block in the production of various fine chemicals, contributing to the advancement of organic chemistry by enabling the creation of novel chemical entities with potential applications in various fields.
Used in Chemical Synthesis:
4,4,6-Trimethyl-1,3-oxazinan-2-one is used as a reagent in organic chemistry research, facilitating the synthesis of complex organic compounds and aiding in the discovery of new chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 27830-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,3 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27830-77:
(7*2)+(6*7)+(5*8)+(4*3)+(3*0)+(2*7)+(1*7)=129
129 % 10 = 9
So 27830-77-9 is a valid CAS Registry Number.

27830-77-9SDS

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 4,4,6-trimethyl-1,3-oxazinan-2-one

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 -
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More Details:27830-77-9 SDS

27830-77-9Downstream Products

27830-77-9Relevant academic research and scientific papers

Interaction of methyl N-(3-oxoalkyl)carbamates, S-methyl-carbamates, and -dithiocarbamates with sodium borohydride. Synthesis of tetrahydro-1,3-oxazin-2-ones and -thiones

Fisyuk,Ryzhova,Unkovskii

, p. 597 - 609 (2007/10/03)

The interaction of N-(3-oxoalkyl)carbamates, -thiocarbamates, and -dithiocarbamates with sodium borohydride has been studied. It was shown that reaction proceeds diastereoselectively, and reductive cyclization with the formation of tetrahydro-1,3-oxazin-2-ones and -thiones may occur. The tend to cyclization of the N-(3-hydroxyalkyl)carbamates, -thiocarbamates, and -dithiocarbamates formed as intermediates depends on the number of substituents in the alkyl chain.

SYNTHESIS OF TETRAHYDRO-1,3-OXAZIN-2-ONES AND -2-THIONES FROM ESTERS OF N-(3-OXOALKYL)CARBAMIC AND -DITHIOCARBAMIC ACIDS

Fisyuk, A. S.,Ryzhova, E. V.,Unkovskii, B. V.

, p. 238 - 242 (2007/10/02)

A study has been made of the interaction of N-(3-oxoalkyl)carbamates and -dithiocarbamates with sodium borohydride; it has been shown that, depending on the pH of the reaction medium, the interaction may produce either tetrahydro-1,3-oxazin-2-ones and -2-

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