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1,6-Dimethyl-3-piperidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

43152-92-7

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43152-92-7 Usage

Common uses

Solvent
Intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds

Physical state

Clear, colorless liquid

Odor

Slightly amine-like

Solubility

Highly soluble in water

Chemical classification

Ketone

Reactivity

Known for its reactivity and versatility in organic synthesis

Safety precautions

Potential to cause irritation to the skin, eyes, and respiratory system
Should be handled with care in a well-ventilated area

Check Digit Verification of cas no

The CAS Registry Mumber 43152-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,5 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 43152-92:
(7*4)+(6*3)+(5*1)+(4*5)+(3*2)+(2*9)+(1*2)=97
97 % 10 = 7
So 43152-92-7 is a valid CAS Registry Number.

43152-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-dimethylpiperidin-3-one

1.2 Other means of identification

Product number -
Other names 1,6-Dimethyl-piperidin-3-one

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:43152-92-7 SDS

43152-92-7Downstream Products

43152-92-7Relevant academic research and scientific papers

The Role of the Nitrogen Atom in the Hydrogenation of Piperidinones and Methylenepiperidines

Senda, Yasuhisa,Okamura, Kazue,Kuwahara, Mayumi,Ide, Masatoshi,Itoh, Hiroki,Ishiyama, Jun-Ichi

, p. 799 - 803 (2007/10/02)

Dimethylpiperidinones and dimethylmethylenepiperidines have been hydrogenated over several Group 8, 9 and 10 transition metal catalysts and the stereochemistry of the products compared with those of the carbocyclic analogues.The results obtained suggest that intramolecular interactions between the nitrogen lone pair and the unsaturated bond play a major role in determining the stereochemistry of hydrogenation.

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