1345403-85-1

Basic information

• Product Name: cyclohex-2-en-1-yl 3-phenoxybenzoate
• Synonyms: cyclohex-2-en-1-yl 3-phenoxybenzoate
• CAS NO: 1345403-85-1
• Molecular Weight: 294.35
• Mol File: 1345403-85-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: cyclohex-2-en-1-yl 3-phenoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: cyclohex-2-en-1-yl 3-phenoxybenzoate(1345403-85-1)
• EPA Substance Registry System: cyclohex-2-en-1-yl 3-phenoxybenzoate(1345403-85-1)

Safety Data

• Hazardous Substances Data: 1345403-85-1(Hazardous Substances Data)

Upstream product

• 13826-35-2 3-Phenoxybenzyl alcohol 
• 110-82-7 cyclohexane 
• 3739-38-6 3-phenoxybenzoic acid 
• 39515-51-0 3-Phenoxybenzaldehyde 
• 1329121-85-8 tert-butyl 3-phenoxybenzoperoxoate 
• 110-83-8 cyclohexene 

Relevant articles and documents

Bu4NI-catalyzed construction of tert-butyl peresters from alcohols

A new method for the synthesis of tert-butyl peresters directly from available alcohols catalyzed by Bu4NI at room temperature in an aqueous system was developed. Additionally, allylic esters could also be obtained by combing this method and Kharasch-Sosnovsky reaction via a two-step one-pot procedure.

Synthesis of tert-butyl peresters from aldehydes by Bu4NI- catalyzed metal-free oxidation and its combination with the Kharasch-Sosnovsky reaction

A new tert-butyl peresters synthesis directly from aldehydes and TBHP was developed via Bu4NI-catalyzed aldehyde C-H oxidation. Mechanistic studies suggest that the protocol proceeds via a radical process. Combining the method with the Kharasch-Sosnovsky reaction offers a practical approach for the synthesis of allylic esters from simple aldehydes and alkenes via a two-step one-pot procedure.