65946-62-5

Basic information

• Product Name: Cyclohexanecarboxaldehyde, 1-(phenylseleno)-
• CAS NO: 65946-62-5
• Molecular Formula: C13H16OSe
• Molecular Weight: 267.229
• Mol File: 65946-62-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Cyclohexanecarboxaldehyde, 1-(phenylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanecarboxaldehyde, 1-(phenylseleno)-(65946-62-5)
• EPA Substance Registry System: Cyclohexanecarboxaldehyde, 1-(phenylseleno)-(65946-62-5)

Safety Data

• Hazardous Substances Data: 65946-62-5(Hazardous Substances Data)

Upstream product

• 53282-55-6 (trimethylsiloxymethylidene)cyclohexane 
• 34837-55-3 Phenylselenyl bromide 
• 2043-61-0 cyclohexanecarbaldehyde 
• 71098-88-9 N-phenylselanylphthalimide 
• 82737-08-4 N-(phenylselanyl)morpholine 
• 57584-86-8 N,N-diethylbenzeneselenamide 
• 1666-13-3 diphenyl diselenide 
• 53198-56-4 1,1-bis(phenylselenenyl)cyclohexane 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 100038-67-3 (E)-3-(1-Phenylselanyl-cyclohexyl)-acrylic acid methyl ester 
• 84782-60-5 1-(1-Phenylselanyl-cyclohexyl)-2-trimethylsilanyl-ethanol 
• 1192-88-7 1-cyclohexene-1-carboxaldehyde 
• 101131-29-7 (1-Phenylselanyl-cyclohexyl)-methanol 
• 100038-77-5 methyl 2-(tert-butoxycarbonylamino)-3-cyclohexylidenepropanoate 
• 81650-64-8 (2-Cyclohexylidene-ethylselanyl)-benzene 
• 84782-65-0 1-Trimethylsilanylmethyl-cyclohexanecarbaldehyde 

Relevant articles and documents

N, N, N -Triphenylselenylisocyanuric Acid (TPSCA): A New Versatile Reagent for α-Phenylselenenylation of Aldehydes and Ketones

A new, versatile reagent, N,N,N-triphenylselenyl-isocyanuric acid (TPSCA) has been prepared, characterized, and used as a source of the electrophilic phenylselenyl group. This relatively stable compound was utilized for an efficient α-selenenylation react

Direct, facile aldehyde and ketone α-selenenylation reactions promoted by L-prolinamide and pyrrolidine sulfonamide organocatalysts

A new catalytic method for direct α-selenenylation reactions of aldehydes and ketones has been developed. The results of exploratory studies have demonstrated that L-prolinamide is an effective catalyst for α-selenenylation reactions of aldehydes, whereas

Synthesis of Spiro-Compounds: Use of Diselenoacetals for Generation of Quaternary Centres by Alkylation and Radical Cyclization

Ketones are readily converted via the corresponding diphenyl diselenoacetals (2) into selenides (5) which undergo radical 5-exo cyclization to spiro-compounds (7) on treatment with triphenyltin hydride and azoisobutyronitrile; an analogous sequence serves