75808-99-0

Basic information

• Product Name: Benzene, [[trans-4-(1,1-dimethylethyl)cyclohexyl]seleno]-
• CAS NO: 75808-99-0
• Molecular Formula: C16H24Se
• Molecular Weight: 295.327
• Mol File: 75808-99-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, [[trans-4-(1,1-dimethylethyl)cyclohexyl]seleno]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [[trans-4-(1,1-dimethylethyl)cyclohexyl]seleno]-(75808-99-0)
• EPA Substance Registry System: Benzene, [[trans-4-(1,1-dimethylethyl)cyclohexyl]seleno]-(75808-99-0)

Safety Data

• Hazardous Substances Data: 75808-99-0(Hazardous Substances Data)

Upstream product

• 126937-59-5 1-methylseleno-1-phenylseleno-4-tert-butyl cyclohexane 
• 126937-58-4 1-methylseleno-1-phenylseleno-4-tert-butyl cyclohexane 
• 126937-56-2 1-phenylseleno-1-perdeuterophenylseleno-4-tert-butyl cyclohexane 
• 71518-68-8 1,1-bis(phenylselenenyl)-4-tert-butylcyclohexane 
• 1666-13-3 diphenyl diselenide 
• 71518-69-9 1,1-bis(methylseleno)-4-tert-butyl cyclohexane 
• 59345-53-8 1-lithio-1-phenylseleno-4-tert-butyl cyclohexane 
• 18508-91-3 methanesulfonic acid 4-tert-butylcyclohexyl ester 
• 2179-79-5 phenyl selenocyanate 
• 937-05-3 cis-4-tert-butyl-1-cyclohexanol 

Downstream Products

• 5009-36-9 cis-1-bromo-4-tert-butylcyclohexane 

Relevant articles and documents

77Se, 13C and 1H NMR Spectra of Phenylselenenylcycloalkanes, -cycloalkenes and Some of Their Selenoxides and 125Te NMR of a Tellurium Analogue

The 77Se, 13C and 1H NMR spectra of 46 mostly new compounds with phenylselenenyl groups attached to carbocycles and of three new corresponding selenoxides and the 125Te NMR of phenyltellurenylcyclohexane are reported.Substituent effects on the chemical sh

Stereoselective Synthesis and Reactions of 1-Seleno-4-tert-Butyl Cyclohexyllithiums

The axial C-Se bond of seleno- and mixed selenoacetals derived from 4-tert-butyl cyclohexanones exhibit a high tendency to be cleaved by n-butyllithium.The resulting 1-seleno-4-tert-butyl cyclohexyllithiums are selectively protonated or selenylated via ax

New Stereoselective Routes from Alcohols to Secondary Alkyl Bromides with Retention of Configuration

Secondary alcohols can be converted into the corresponding bromides with high stereoselective retention of configuration; this two-step process proceeds by a double inversion involving the intermediate selenides.