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3-(hydroxymethyl)-1-methyl-2-Piperidinone is a chemical compound with the molecular formula C7H13NO2. It is a derivative of piperidinone and contains a hydroxymethyl group and a methyl group attached to the piperidinone ring. 3-(hydroxymethyl)-1-methyl-2-Piperidinone has significant industrial and pharmaceutical relevance due to its versatile and useful properties for synthesis and production purposes.

944276-44-2

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944276-44-2 Usage

Uses

Used in Pharmaceutical Industry:
3-(hydroxymethyl)-1-methyl-2-Piperidinone is used as an intermediate in the synthesis of pharmaceuticals for its potential applications as a building block for the production of various drugs and synthetic compounds.
Used in Organic Chemical Industry:
3-(hydroxymethyl)-1-methyl-2-Piperidinone is used as an intermediate in the synthesis of organic chemicals, contributing to the development of new compounds and materials.
Used as a Solvent in Chemical Processes:
3-(hydroxymethyl)-1-methyl-2-piperidinone may be used as a solvent in chemical processes, facilitating various reactions and contributing to the efficiency of production methods.

Check Digit Verification of cas no

The CAS Registry Mumber 944276-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,2,7 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 944276-44:
(8*9)+(7*4)+(6*4)+(5*2)+(4*7)+(3*6)+(2*4)+(1*4)=192
192 % 10 = 2
So 944276-44-2 is a valid CAS Registry Number.

944276-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxymethyl)-1-methylpiperidin-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:944276-44-2 SDS

944276-44-2Relevant academic research and scientific papers

Novel spiroheterocycles by aziridination of α-methylene-γ- and -δ-lactams

Loreto, M. Antonietta,Migliorini, Antonella,Tardella, P. Antonio,Gambacorta, Augusto

, p. 2365 - 2371 (2007)

New potentially bioactive α-spiroaziridino-γ- and -δ-lactams have been prepared by treatment of α-methylene-γ- and -δ-lactams with ethyl N-([(4-nitrophenyl)sulfonyl]oxy)-carbamate (NsONHCO2Et) in the presence of CaO. These compounds, through reductive aziridine ring opening, can be intermediates for the synthesis of α- and β-aminolactams, which are useful as conformational constraints in peptides. The above procedure has been successfully extended to one α-methyleneoxindole to obtain a new spirooxindole derivative, a potential precursor of natural alkaloids. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

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