benzyl N-(3-methylazetidin-3-yl)carbamate hydrochloride
$350.00
CAS No.: 1951441-46-5
Catalog No.: 195493
Purity: 95%
MF: C12H17ClN2O2
MW: 256.733
Storage: 2-8 degree Celsius
SMILES: Cl.CC1(CNC1)NC(OCC1=CC=CC=C1)=O
Catalog No.: 195493
Purity: 95%
MF: C12H17ClN2O2
MW: 256.733
Storage: 2-8 degree Celsius
SMILES: Cl.CC1(CNC1)NC(OCC1=CC=CC=C1)=O
benzyl N-(3-methylazetidin-3-yl)carbamate hydrochloride; CAS No.: 1951441-46-5; benzyl N-(3-methylazetidin-3-yl)carbamate hydrochloride. PROPERTIES: Benzyl N-(3-methylazetidin-3-yl)carbamate hydrochloride appears as a white to off-white crystalline powder with a slight odor. Its molecular formula is C12H16ClN2O2, corresponding to a molecular weight of approximately 265.73 g/mol. The compound exhibits a melting point in the range of 200-203 C and demonstrates good solubility in water and polar organic solvents such as methanol and ethanol. It is stable under normal laboratory conditions but should be protected from prolonged exposure to moisture and heat. Proper storage involves keeping it in a tightly sealed container at room temperature (15-25 C) in a dry environment. Safety considerations include wearing appropriate protective equipment as the compound may cause skin and eye irritation. Inhalation of dust should be avoided, and in case of accidental exposure, thorough washing with water and medical consultation is advised. APPLICATIONS: Benzyl N-(3-methylazetidin-3-yl)carbamate hydrochloride serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly in the preparation of certain antidepressants and antipsychotics. Its azetidine and benzyl groups provide structural features important for receptor binding and bioactivity. In biochemical research, it functions as a building block for creating enzyme inhibitors and prodrugs. Additionally, it finds application in the development of fluorescent probes for bioimaging, where its benzyl group allows for selective labeling of biological targets such as proteins and lipids. The compound is also employed in the synthesis of agrochemicals, though specific applications in this area are limited to non-agricultural research settings.
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