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297172-01-1

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297172-01-1 Usage

General Description

(R)-ethyl 3-Methylpiperidine-3-carboxylate is a chemical compound with the molecular formula C11H21NO2. It is a chiral molecule with a specific stereochemistry, denoted by the (R) prefix. (R)-ethyl 3-Methylpiperidine-3-carboxylate belongs to the class of piperidine carboxylic acid esters and is commonly used as an intermediate or building block in the synthesis of pharmaceuticals and organic compounds. It may also have applications in chemical research and development. Caution should be exercised when handling this compound as it may be hazardous if not used properly and in accordance with safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 297172-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,7 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 297172-01:
(8*2)+(7*9)+(6*7)+(5*1)+(4*7)+(3*2)+(2*0)+(1*1)=161
161 % 10 = 1
So 297172-01-1 is a valid CAS Registry Number.

297172-01-1SDS

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 ethyl (3R)-3-methylpiperidine-3-carboxylate

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:297172-01-1 SDS

297172-01-1Relevant articles and documents

Synthesis of a potent hNK-1 receptor antagonist via an SN2 reaction of an enantiomerically pure α-alkoxy sulfonate

Nelson, Todd D.,Rosen, Jonathan D.,Smitrovich, Jacqueline H.,Payack, Joseph,Craig, Bridgette,Matty, Louis,Huffman, Mark A.,McNamara, James

, p. 55 - 58 (2007/10/03)

(Chemical Equation Presented) The concise synthesis of a stereochemically rich hNK-1 receptor antagonist is described. The synthesis is highlighted by an SN2 reaction of an enantiomerically pure α-alkoxy sulfonate (orthogonally protected butane triol), which was prepared by utilizing salen-mediated hydrolytic kinetic resolution technology. A stereocontrolled acetalization was employed to connect two enantiomerically pure fragments with a high degree of diastereoselectivity.

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