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2-Piperidinone,5-methyl-3-methylene-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

514847-19-9

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514847-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 514847-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,4,8,4 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 514847-19:
(8*5)+(7*1)+(6*4)+(5*8)+(4*4)+(3*7)+(2*1)+(1*9)=159
159 % 10 = 9
So 514847-19-9 is a valid CAS Registry Number.

514847-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-3-methylidenepiperidin-2-one

1.2 Other means of identification

Product number -
Other names 2-Piperidinone,5-methyl-3-methylene

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:514847-19-9 SDS

514847-19-9Downstream Products

514847-19-9Relevant academic research and scientific papers

Ruthenium-Catalyzed Cyclocarbonylation of Allenyl Alcohols and Amines: Selective Synthesis of Lactones and Lactams

Yoneda, Eiji,Zhang, Shi-Wei,Zhou, Da-Yang,Onitsuka, Kiyotaka,Takahashi, Shigetoshi

, p. 8571 - 8576 (2007/10/03)

Allenyl alcohols such as 4-hydroxybuta-1,2-dienes and 5-hydroxypenta-1,2-dienes having a variety of substituents undergo cyclocarbonylation in the presence of a ruthenium catalyst under mild conditions selectively to give five- and six-membered lactones in a high yield with 100% atom economy. 5-Aminopenta-1,2-dines are also cyclocarbonylated to give γ-lactams. A possible carbonylation mechanism involving a ruthenium cluster intermediate is proposed on the basis of experimental results.

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