Azetidine-3-carboxylic acid hydrochloride

Base Information

• Chemical Name: Azetidine-3-carboxylic acid hydrochloride
• CAS No.: 102624-96-4
• Molecular Formula: C4H8ClNO2
• Molecular Weight: 137.5648
• Hs Code.: 2933990090
• European Community (EC) Number: 676-204-4
• DSSTox Substance ID: DTXSID90538625
• Mol file: 102624-96-4.mol

Synonyms:102624-96-4;AZETIDINE-3-CARBOXYLIC ACID HYDROCHLORIDE;azetidine-3-carboxylic acid hcl;Azetidine-3-carboxylicacidhydrochloride;3-Azetidinecarboxylic acid HCl;3-Azetidinecarboxylic acid, hydrochloride (1:1);azetidine-3-carboxylic acid;hydrochloride;Azetidine-3-carboxylic acid, HCl;3-Azetidinecarboxylicacid, hydrochloride (1:1);3-Azetidinecarboxylic acid hydrochloride;Azetidine-3-carboxylic acid inverted exclamation mark currencyHCl;SCHEMBL563782;AMY4825;DTXSID90538625;RNIZUCJGSDJAOQ-UHFFFAOYSA-N;MFCD06796562;AKOS015848389;SB50862;AS-36969;CS-0067915;azetidine-3-carboxylic acid hydrochloride salt;A13577;3-azetidinecarboxylic acid methyl ester hydrochloride;J-519620;Q-103129;Azetidine-3-carboxylic acid--hydrogen chloride (1/1)

Chemical Property of Azetidine-3-carboxylic acid hydrochloride

Chemical Property:

• Vapor Pressure: 0.00218mmHg at 25°C
• Boiling Point: 268.5 °C at 760 mmHg
• Flash Point: 116.2 °C
• PSA: 49.33000
• LogP: 0.42120
• Storage Temp.: Sealed in dry,Room Temperature
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 137.0243562
• Heavy Atom Count: 8
• Complexity: 87.7

Purity/Quality:

99% ^*data from raw suppliers

Azetidine-3-carboxylicacidhydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(CN1)C(=O)O.Cl
• Use Description: Azetidine-3-carboxylic acid hydrochloride, also known as ACBC hydrochloride, has various applications across different fields. In the pharmaceutical industry, it serves as a crucial intermediate in the synthesis of pharmaceutical compounds, particularly for drugs with applications in neuroscience and central nervous system disorders. ACBC derivatives are often employed in medicinal chemistry to develop potential therapies for conditions like Alzheimer's disease and schizophrenia. Additionally, in the field of organic chemistry, ACBC hydrochloride is utilized as a versatile building block for the synthesis of various heterocyclic compounds, which find applications in agrochemicals and materials science. Its multifunctional role in drug development and chemical synthesis underscores its significance in advancing both the pharmaceutical and chemical industries.