69930-99-0

Basic information

• Product Name: 1,1-(bisphenylseleno)cyclopropane
• CAS NO: 69930-99-0
• Molecular Weight: 352.196
• Mol File: 69930-99-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,1-(bisphenylseleno)cyclopropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-(bisphenylseleno)cyclopropane(69930-99-0)
• EPA Substance Registry System: 1,1-(bisphenylseleno)cyclopropane(69930-99-0)

Safety Data

• Hazardous Substances Data: 69930-99-0(Hazardous Substances Data)

Upstream product

• 69930-97-8 C₁₅H₁₅ClSe₂ 
• 75-21-8 oxirane 
• 20343-90-2 bis(phenylseleno)methane 
• 645-96-5 Benzeneselenol 
• 107-02-8 acrolein 

Downstream Products

• 72485-62-2 Phenyl-cyclopropyl-selenid 
• 78814-40-1 [1-(2-Octyl-dec-1-enyl)-cyclopropylselanyl]-benzene 
• 79011-91-9 [((Z)-1-Oct-1-enyl)-cyclopropylselanyl]-benzene 
• 78814-41-2 (1-Cyclobutylidenemethyl-cyclopropylselanyl)-benzene 
• 78814-55-8 2-Methylselanyl-2-octyl-1-(1-phenylselanyl-cyclopropyl)-decan-1-ol 
• 78814-50-3 2-Phenylselanyl-1-(1-phenylselanyl-cyclopropyl)-octan-1-ol 
• 78814-49-0 2-Methylselanyl-1-(1-phenylselanyl-cyclopropyl)-octan-1-ol 
• 78814-56-9 (1-Methylselanyl-cyclobutyl)-(1-phenylselanyl-cyclopropyl)-methanol 
• 78814-30-9 1-phenylselanylcyclopropanecarbaldehyde 
• 28622-61-9 butyl phenyl selenide 
• 118526-88-8 phenyl-<(1-phenylseleno)cyclopropyl>-methanol 
• 72485-60-0 1-Phenylseleno-1-carboxycyclopropan 

Relevant articles and documents

SYNTHESIS OF α-SELENOALKYLLITHIUM COMPOUNDS

α-Phenylselenoalkyllithiums and α-methylselenoalkyllithiums have been prepared from the corresponding selenoacetals and alkyllithiums.Several features of this reaction are disclosed.For example, the reaction is more readily achieved on phenylselenoacetals than on methylseleno analogues.Those derived from hindered carbonyl compounds are less readily cleaved. s-BuLi/THF proved superior to n-BuLi in THF, itself better than n-BuLi in ether.

PREPARATION OF 3-HYDROXYL-VINYL SELENIDES AND 1,3-BIS(SELENO)-PROPENES

Z and E 3-hydroxy-vinyl selenides can be prepared with very high stereoselectivity respectively by nucleophilic addition of selenolates to propargyl alcohols and by selenylation followed by LiAlH4 reduction of the same propargyl alcohols. 1,3-Bis(seleno)-