1345403-82-8

Basic information

• Product Name: cyclohex-2-en-1-yl 2-naphthoate
• Synonyms: cyclohex-2-en-1-yl 2-naphthoate
• CAS NO: 1345403-82-8
• Molecular Weight: 252.313
• Mol File: 1345403-82-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: cyclohex-2-en-1-yl 2-naphthoate(CAS DataBase Reference)
• NIST Chemistry Reference: cyclohex-2-en-1-yl 2-naphthoate(1345403-82-8)
• EPA Substance Registry System: cyclohex-2-en-1-yl 2-naphthoate(1345403-82-8)

Safety Data

• Hazardous Substances Data: 1345403-82-8(Hazardous Substances Data)

Upstream product

• 110-83-8 cyclohexene 
• 93-09-4 naphthalene-2-carboxylate 
• 1592-38-7 2-Naphthalenemethanol 
• 110-82-7 cyclohexane 
• 66-99-9 β-naphthaldehyde 
• 34304-74-0 tert-butyl naphthalene-2-carboperoxoate 

Relevant articles and documents

Copper porphyrin-catalyzed cross dehydrogenative coupling of alkanes with carboxylic acids: Esterification and decarboxylation dual pathway

A dual-functional copper porphyrin-catalyzed cross dehydrogenative coupling (CDC) of carboxylic acids with alkanes was reported firstly. The reaction gives allylic esters or alkylalkenes depending on the carboxylic acid substrates. Copper porphyrin catalyzed CDC method has the superiority of short reaction time, good functional group tolerance, base and solvent free, producing target products in an atom-economic manner.

Copper porphyrin as efficient catalysts for esterification of allyl sp3 C–H bond with carboxylic acid

We described that copper 5,10,15,20-tetrakis (ethoxycarbonyl)porphyrin (TECP) catalyzed oxidative cross dehydrogenative coupling of allyl sp3 C–H bond with acid for the synthesis of allyl esters in a homogeneous system. This reaction proceeded

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.