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3-Pyrrolidinecarboxylicacid,1-methyl-,methylester,(3S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

226088-57-9

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226088-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226088-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,0,8 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 226088-57:
(8*2)+(7*2)+(6*6)+(5*0)+(4*8)+(3*8)+(2*5)+(1*7)=139
139 % 10 = 9
So 226088-57-9 is a valid CAS Registry Number.

226088-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-1-methyl-pyrrolidine-3-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names (S)-1-Methyl-pyrrolidine-3-carboxylic 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:226088-57-9 SDS

226088-57-9Downstream Products

226088-57-9Relevant academic research and scientific papers

Ex-chiral pool synthesis and pharmacological aspects of 3- pyrrolidinylisoxazoles

Thomas,Ohnmacht,Zahn,Mohr,Gmeiner, Peter

, p. 248 - 250 (2007/10/03)

Employing the dopamine autoreceptor agonist (-)-3-PPP (3) as well as the cholinergic receptor ligands 4 and 5 as lead compounds the 3- pyrrolidinylisoxazoles 2a,b as well as its optical antipodes ent-2a,b were synthesized from (R)-aspartic acid (6) and (S)-aspartic acid (ent-6), respectively. Pharmacological properties of the target compounds were evaluated employing dopamine D2 receptor binding studies and functional experiments on muscarinic M2 receptors.

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