4392-27-2

Basic information

• Product Name: 1-phenyl-3-chloro-1,2-epoxypropane
• Synonyms: 1-phenyl-3-chloro-1,2-epoxypropane
• CAS NO: 4392-27-2
• Molecular Weight: 168.623
• Mol File: 4392-27-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-phenyl-3-chloro-1,2-epoxypropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-3-chloro-1,2-epoxypropane(4392-27-2)
• EPA Substance Registry System: 1-phenyl-3-chloro-1,2-epoxypropane(4392-27-2)

Safety Data

• Hazardous Substances Data: 4392-27-2(Hazardous Substances Data)

Upstream product

• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 2687-12-9 cinnamyl chloride 
• 93-59-4 Perbenzoic acid 

Downstream Products

• 184046-30-8 trans-2-(chloromethyl)-3-phenyloxirane 
• 1137968-48-9 (1R,2R)-3-chloro-1-phenylpropane-1,2-diol 
• 107643-29-8 (1R,2S)-1-phenylglycidol 
• 937-38-2 1-chloro-3-phenylpropan-2-one 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 935-04-6 benzyl vinyl ether 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 22168-19-0 1-Phenyl-1-fluor-3-chlor-propanol-⁽²⁾ 

Relevant articles and documents

FUNCTIONAL GROUP MODIFICATION VIA ORGANOTELLURIUM CHEMISTRY. SYNTHESIS OF ALLYL ALCOHOLS FROM CHLOROMETHYLOXIRANES.

Treatment of 2-substitued-2-chloromethyloxiranes with telluride ion gives 2-substitued allyl alcohols, presumably through an epitelluride intermediate.

Cyclic benzamidines as orally efficacious NR2B-selective NMDA receptor antagonists

A novel series of cyclic benzamidines was synthesized and shown to exhibit NR2B-subtype selective NMDA antagonist activity. Compound 29 is orally active in a carrageenan-induced rat hyperalgesia model of pain.

A Mild and Efficient Epoxidation of Olefins Using in Situ Generated Dimethyldioxirane at High pH

-