7468-30-6

Basic information

• Product Name: 1-Benzyl-3,3-dimethyl-4-phenylazetidine-2-one
• Synonyms: 3,3-Dimethyl-4-phenyl-1-(phenylmethyl)azetidin-2-one;1-Benzyl-3,3-dimethyl-4-phenylazetidine-2-one
• CAS NO: 7468-30-6
• Molecular Formula: C₁₈H₁₉NO
• Molecular Weight: 0
• Mol File: 7468-30-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 433.5°C at 760 mmHg
• Flash Point: 176.3°C
• Appearance: /
• Density: 1.108g/cm³
• Vapor Pressure: 1.02E-07mmHg at 25°C
• Refractive Index: 1.586
• CAS DataBase Reference: 1-Benzyl-3,3-dimethyl-4-phenylazetidine-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Benzyl-3,3-dimethyl-4-phenylazetidine-2-one(7468-30-6)
• EPA Substance Registry System: 1-Benzyl-3,3-dimethyl-4-phenylazetidine-2-one(7468-30-6)

Safety Data

• Hazardous Substances Data: 7468-30-6(Hazardous Substances Data)

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 49, p. 396, 1984 DOI: 10.1021/jo00176a040

InChI:InChI=1/C18H19NO/c1-18(2)16(15-11-7-4-8-12-15)19(17(18)20)13-14-9-5-3-6-10-14/h3-12,16H,13H2,1-2H3

Upstream product

• 73521-09-2 3-benzylamino-2,2-dimethyl-3-phenyl-propionic acid 
• 859953-35-8 3-(benzyl-isobutyryl-amino)-2,2-dimethyl-3-phenyl-propionic acid 
• 598-26-5 dimethylketene 
• 780-25-6 N-benzylidene benzylamine 
• 600-00-0 ethyl 2-bromoisobutyrate 
• 81357-56-4 Thioisobutyric acid S-pyridin-2-yl ester 
• 88296-01-9 2-benzyl-4-methyl-1-phenyl-3-oxo-6-thia-2-azabicyclo<2.2.0>hexane 
• 121-69-7 N,N-dimethyl-aniline 
• 27845-50-7 (E)-N-benzylidenebenzylamine 

Downstream Products

• 73521-09-2 3-benzylamino-2,2-dimethyl-3-phenyl-propionic acid 
• 22606-97-9 1-benzyl-3,3-dimethyl-2-phenylazetidine 

Relevant articles and documents

Synthesis of β-lactams and β-aminoesters via high intensity ultrasound-promoted Reformatsky reactions

Reformatsky reactions of an imine, an α-bromoester, zinc dust and a catalytic amount of iodine in dioxane under high intensity ultrasound (HIU) irradiation from an ultrasonic probe are explored. A series of 16 aldimines with varying electronic demands is

A New Synthesis of β-Lactams: 3-Oxo-6-thia-2-azabicyclohexanes via Photochemical Reactions of N-(Thiobenzoyl)methacrylamides

Irradiation of N-(thiobenzoyl)methacrylamides in benzene gave thietan-fused β-lactams in good yields, and these were converted to other β-lactams by reduction or oxidation.