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1,2-Piperidinedicarboxylic acid, 4-(formyloxy)-, 2-methyl 1-(phenylmethyl) ester, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

475504-28-0

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475504-28-0 Usage

Derived from piperidine

The compound is based on a heterocyclic amine called piperidine.

Methyl ester

The compound is a methyl ester of 1,2-piperidine dicarboxylic acid.

Formyloxy group

A formyloxy (-CHO) group is attached to the 4th position of the piperidine ring.

Phenylmethyl group

A phenylmethyl (-CH2C6H5) group is attached to the 1st position of the piperidine ring.

(2S)-Configuration

The compound has a specific stereochemistry, with the S-configuration at the 2nd position of the piperidine ring.

Pharmacological properties

The compound may have potential pharmacological properties and could be used as a building block for the synthesis of various pharmaceuticals or organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 475504-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,5,0 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 475504-28:
(8*4)+(7*7)+(6*5)+(5*5)+(4*0)+(3*4)+(2*2)+(1*8)=160
160 % 10 = 0
So 475504-28-0 is a valid CAS Registry Number.

475504-28-0SDS

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 4-formyloxy-(S)-pipecolic acid methyl ester

1.2 Other means of identification

Product number -
Other names (2S)-4-formylpipecolic acid methyl ester

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:475504-28-0 SDS

475504-28-0Relevant academic research and scientific papers

Use of hydrolases for the synthesis of cyclic amino acids

Lloyd, Richard C.,Lloyd, Michael C.,Smith, Mark E. B.,Holt, Karen E.,Swift, Jonathan P.,Keene, Philip A.,Taylor, Stephen J. C.,McCague, Raymond

, p. 717 - 728 (2004)

The synthesis of several cyclic amino acids that have all the necessary structural features to make them ideal scaffolds for use in medicinal chemistry is described. A key step in each synthesis is the use of hydrolase enzymes to define a chiral centre. I

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