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1212293-24-7

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1212293-24-7 Usage

Uses

(S)-1-Benzylpyrrolidine-3-carboxylic Acid Hydrochloride is used as a reactant in the preparation of N-indolylalkyl heteroarylcarboxamide derivatives as TAU-induced toxicity inhibitors useful in the treatment of neurodegenerative diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1212293-24-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,2,2,9 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1212293-24:
(9*1)+(8*2)+(7*1)+(6*2)+(5*2)+(4*9)+(3*3)+(2*2)+(1*4)=107
107 % 10 = 7
So 1212293-24-7 is a valid CAS Registry Number.

1212293-24-7SDS

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 (3S)-1-benzylpyrrolidine-3-carboxylic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names (S)-1-N-benzyl-A-proline hydrochloride

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:1212293-24-7 SDS

1212293-24-7Relevant articles and documents

A practical ex-chiral-pool synthesis of β-proline and homo-β-proline

Thomas, Christoph,Orecher, Florian,Gmeiner, Peter

, p. 1491 - 1496 (1998)

Starting from aspartic acid an efficient synthesis of enantiomerically pure β-proline and homo-β-proline is described. The key step of the synthesis includes formation of the 1,4-biselectrophile 6, followed by rearrangement via the aziridinium intermediate 7 and ring closure to give the pyrrolidinium salt 9a which can serve as a common precursor for both target compounds.

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