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2133-35-9

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2133-35-9 Usage

General Description

L-Azetidine-2-carboxylic acid HCL is a chemical compound that belongs to the class of organic compounds known as proline and derivatives. It is a crystalline solid with a molecular formula of C5H9NO2.HCl. L-AZETIDINE-2-CARBOXYLIC ACID HCL is commonly used in the synthesis of pharmaceuticals and as a building block for the preparation of various chemical compounds. It may also have potential applications in the field of agricultural chemicals and biotechnology. L-Azetidine-2-carboxylic acid HCL is of interest in scientific research for its unique molecular structure and versatile chemical reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 2133-35-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2133-35:
(6*2)+(5*1)+(4*3)+(3*3)+(2*3)+(1*5)=49
49 % 10 = 9
So 2133-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO2.ClH/c6-4(7)3-1-2-5-3;/h3,5H,1-2H2,(H,6,7);1H/t3-;/m0./s1

2133-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name azetidine-2-carboxylic acid hydrochloride

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:2133-35-9 SDS

2133-35-9Upstream product

2133-35-9Downstream Products

2133-35-9Relevant articles and documents

Methods for producing N-protected-azetidine-2-carboxylic acids

-

, (2008/06/13)

There is disclosed a method for producing an essentially enantiomerically pure N-protected-azetidine-2-carboxylic acid of formula (1): which method is characterized by: subjecting a crude enantiomerically excess N-protected-azetidine-2-carboxylic acid comprising said enantiomer represented by formula (1) in excess to the other enantiomer thereof to crystallization in an organic solvent selected from aromatic hydrocarbon, aliphatic ether, aliphatic alcohol, aliphatic ketone, aliphatic nitrile, aliphatic amide, aliphatic sulfoxide, aliphatic ester and a mixed solvent thereof, wherein R is: an optionally substituted alkyl, alicyclic or alicyclicalkyl group, an optionally substituted alkenyl group, an optionally substituted aryl group, an optionally substituted heteroaryl group, or a dialkylamino group, and absolute configuration of the asterisked asymmetric carbon atom is S or R.

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