56414-33-6

Basic information

• Product Name: 4-Octanol, 5-(phenylseleno)-
• CAS NO: 56414-33-6
• Molecular Formula: C14H22OSe
• Molecular Weight: 285.288
• Mol File: 56414-33-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-Octanol, 5-(phenylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Octanol, 5-(phenylseleno)-(56414-33-6)
• EPA Substance Registry System: 4-Octanol, 5-(phenylseleno)-(56414-33-6)

Safety Data

• Hazardous Substances Data: 56414-33-6(Hazardous Substances Data)

Upstream product

• 14850-23-8 trans-4-Octene 
• 34837-55-3 Phenylselenyl bromide 
• 7642-15-1 (Z)-oct-4-ene 
• 5707-04-0 Phenylselenyl chloride 
• 1439-06-1 4,5-epoxyoctane 
• 1111071-92-1 phenylselenyl zinc chloride 
• 1666-13-3 diphenyl diselenide 
• 23974-72-3 sodium phenylselenide 

Downstream Products

• 14850-23-8 trans-4-Octene 
• 58856-09-0 C₁₄H₂₂O₂Se 

Relevant articles and documents

Iodide-promoted deselenylation of β-chloro-and β-oxyselenides to form alkenes and selenenyl iodides

Deselenylation reaction of β-chloro-and β-oxyselenides proceeded efficiently by treatment with tetrabutylammonium iodide (TBAI) to afford alkenes in good yields. It was established that selenenyl iodides were formed in these reactions. Catalytic transformation of β-chloro-and β-oxyselenides to alkenes was also developed.

Iodosobenzene diacetate and diphenyl diselenide: An electrophilic selenenylating agent of double bonds

Phenylseleno-acetoxylation, hydroxylation, etherification and lactonization products are obtained in good yields from the reaction of alkenes with diphenyl diselenide and iodosobenzene diacetate, in acetonitrile.

SYNTHESIS OF CONJUGATED NITROALKENES VIA NITROSELENENYLATION OF ALKENES

Addition of silver nitrite to 2-bromoalkyl phenyl selenide in the presence of mercury(II)chloride afforded 2-nitroalkyl phenyl selenide, wich upon oxidative deselenenylation provided the conjugated nitroalkene in excellent yield.