2133-35-9 Usage
Uses
Used in Pharmaceutical Synthesis:
L-Azetidine-2-carboxylic acid HCL is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with improved therapeutic properties.
Used in Chemical Compound Preparation:
L-Azetidine-2-carboxylic acid HCL is used as a building block in the preparation of various chemical compounds, enabling the creation of a wide range of molecules with diverse applications.
Used in Agricultural Chemicals:
L-Azetidine-2-carboxylic acid HCL is used in the development of agricultural chemicals, potentially contributing to the creation of more effective and environmentally friendly products for crop protection and enhancement.
Used in Biotechnology:
L-Azetidine-2-carboxylic acid HCL is used in biotechnological applications, where its unique molecular structure and reactivity can be leveraged to develop innovative solutions in areas such as enzyme catalysis, drug delivery, and bioactive molecule design.
Used in Scientific Research:
L-Azetidine-2-carboxylic acid HCL is utilized in scientific research for its unique molecular structure and versatile chemical reactivity, providing a valuable tool for exploring new chemical reactions and understanding the fundamental principles of organic chemistry.
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
2133-35-9Relevant academic research and scientific papers
Methods for producing N-protected-azetidine-2-carboxylic acids
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, (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.
