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224184-14-9

2-Piperidinone,5-(methoxymethoxy)-6-methyl-,(5S,6S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

224184-14-9

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224184-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 224184-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,1,8 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 224184-14:
(8*2)+(7*2)+(6*4)+(5*1)+(4*8)+(3*4)+(2*1)+(1*4)=109
109 % 10 = 9
So 224184-14-9 is a valid CAS Registry Number.

224184-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5S,6S)-5-Methoxymethoxy-6-methyl-piperidin-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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:224184-14-9 SDS

224184-14-9Relevant articles and documents

Construction of 4a,8a-cis-octahydroquinolin-7-one core using an intramolecular aldol type of cyclization: An application to enantioselective total synthesis of lepadin B

Toyooka, Naoki,Okumura, Maiko,Takahata, Hiroki,Nemoto, Hideo

, p. 10673 - 10684 (2007/10/03)

An intramolecular aldol type of cyclization of the piperidine derivative 1 proceeded in highly stereoselective manner to afford the desired 4a,8a-cis- octahydroquinolin-7-one. This key step involves a feature of the use of A((1.3)) strain as a control element, in biasing 1 towards the conformer desired for the above cyclization. An application of this aldol reaction to enantioselective total synthesis of the marine alkaloid lepadin B is also described.

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