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62686-97-9

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62686-97-9 Usage

General Description

2-(piperidin-2-ylidene)cyclopentane-1,3-dione is a chemical compound that consists of a cyclopentane ring with two substituents - a piperidine ring and a carbonyl group. It is a cyclic diketone with a piperidine ring attached to one of its carbon atoms. 2-(piperidin-2-ylidene)cyclopentane-1,3-dione is used in organic synthesis and pharmaceutical research as a building block for the creation of various chemical compounds and pharmaceutical products. Its unique structure and reactivity make it a valuable component in the development of new drugs and organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 62686-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,8 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62686-97:
(7*6)+(6*2)+(5*6)+(4*8)+(3*6)+(2*9)+(1*7)=159
159 % 10 = 9
So 62686-97-9 is a valid CAS Registry Number.

62686-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-piperidin-2-ylidenecyclopentane-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-piperidin-2-ylidene-cyclopentane-1,3-dione

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:62686-97-9 SDS

62686-97-9Downstream Products

62686-97-9Relevant articles and documents

Boric acid: a new regiospecific decarboxylating agent. Syntheses of cyclic imines, β-enaminones, and β-enaminodiketones from β-enaminoesters

Delbecq, Philippe,Bacos, Daniel,Celerier, Jean Pierre,Lhommet, Gerard

, p. 1201 - 1206 (2007/10/02)

The synthesis of cyclic imines 2, β-enaminones 6, and β-enaminodiketones 7 is described.Regio- and stereospecific thermolysis of β-enaminoesters 4 with boric acid permit these preparations in generally good yields. Key words: boric acid, cyclic β-enaminoesters, decarboxylation, cyclic imines, cyclic β-enaminones.

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