6421-12-1

Basic information

• Product Name: Carbonic acid, cyclohexyl phenyl ester
• CAS NO: 6421-12-1
• Molecular Formula: C13H16O3
• Molecular Weight: 220.268
• Mol File: 6421-12-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Carbonic acid, cyclohexyl phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonic acid, cyclohexyl phenyl ester(6421-12-1)
• EPA Substance Registry System: Carbonic acid, cyclohexyl phenyl ester(6421-12-1)

Safety Data

• Hazardous Substances Data: 6421-12-1(Hazardous Substances Data)

Upstream product

• 1561-49-5 dicyclohexyl peroxydicarbonate 
• 18678-65-4 isocyanatotriphenylsilane 
• 71-43-2 benzene 
• 1885-14-9 phenyl chloroformate 
• 108-93-0 cyclohexanol 
• 1202680-24-7 phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate 
• 931-50-0 cyclohexylmagnesium bromide 

Relevant articles and documents

Alkyl Carbazates for Electrochemical Deoxygenative Functionalization of Heteroarenes

The C?O bond cleavage for activation of alcohols is synthetically useful and practically challenging. This work describes carbazate as a new type of electrochemically activated alkylating agent derived from ubiquitous alcohols for direct functionalization of heteroarenes under mild electrolytic conditions. The simple undivided cell at low oxidative potentials with carbon/platinum electrode set-ups offers excellent substrate tolerance, affording a variety of primary, secondary and tertiary alkyl-decorated heterocycles in good chemical yields. Furthermore, the mechanism for this electrochemical deoxyalkylation reaction has been investigated.

Synthesis of organic carbonates with alkyl/aryl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylates and ROH/AlCl3under ambient condition

We demonstrated the synthesis of organic carbonates using alkyl/aryl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylates and alcohol in the presence of aluminum chloride. Alkyl/aryl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylates were reacted with alcohol in the presence of AlCl3 in toluene at room temperature to afford the corresponding unsymmetric and symmetric organic carbonates in good to excellent yields. These are efficient and convenient processes. Alkyl/aryl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylates are solid, stable and non-toxic CO2/CO2R(Ar) source. It is noteworthy that the reaction is carry out under an ambient and acidic conditions, the easy-to prepare and readily available starting materials and the quantitative isolation of reusable 4,5-dichloropyridazin-3(2H)-one.

REACTIONS OF ISOCYANATOTRIPHENYL-STANNANE AND SILANE WITH DICYCLOHEXYL PEROXYDICARBONATE

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