25566-04-5

Basic information

• Product Name: 3-Phenylazetidin-3-ol
• Synonyms: 3-Phenylazetidin-3-ol;3-Phenyl-3-azetidinol
• CAS NO: 25566-04-5
• Molecular Formula: C9H11NO
• Molecular Weight: 149.19
• Mol File: 25566-04-5.mol
• Article Data: 0

Chemical Properties

• Melting Point: 154-156℃
• Boiling Point: 265℃
• Flash Point: 125℃
• Appearance: /
• Density: 1.178
• CAS DataBase Reference: 3-Phenylazetidin-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Phenylazetidin-3-ol(25566-04-5)
• EPA Substance Registry System: 3-Phenylazetidin-3-ol(25566-04-5)

Safety Data

• Hazardous Substances Data: 25566-04-5(Hazardous Substances Data)

Usage

Description

3-Phenylazetidin-3-ol, also known as S-(-)-3-phenylazetidin-3-ol, is a chiral compound belonging to the class of azetidines. It is an organochlorine compound and a chiral auxiliary used in asymmetric synthesis. 3-Phenylazetidin-3-ol has a four-membered azetidine ring with a phenyl group attached to the third carbon and a hydroxyl group at the second carbon. It is a versatile building block in organic synthesis and can be utilized in the preparation of biologically active molecules and pharmaceuticals. Its application in asymmetric synthesis makes it a valuable tool for the development of new drugs and efficient chemical processes.

Uses

Used in Pharmaceutical Industry:
3-Phenylazetidin-3-ol is used as a chiral building block for the synthesis of biologically active molecules and pharmaceuticals. Its unique structure and chirality enable the development of enantioselective reactions and the production of chiral compounds with specific biological activities.
Used in Organic Synthesis:
3-Phenylazetidin-3-ol is used as a versatile building block in organic synthesis for the preparation of various organic compounds. Its four-membered azetidine ring and functional groups allow for a wide range of chemical reactions and transformations, making it a useful intermediate in the synthesis of complex organic molecules.
Used in Asymmetric Synthesis:
3-Phenylazetidin-3-ol is used as a chiral auxiliary in asymmetric synthesis to control the stereochemistry of chemical reactions. Its presence can induce enantioselectivity, leading to the formation of chiral products with high enantiomeric purity. This application is particularly valuable in the development of new drugs and efficient chemical processes that require specific stereochemistry for biological activity.