63831-77-6

Basic information

• Product Name: (1-METHYLENE-HEPTYLSELANYL)-BENZENE
• Synonyms: (1-METHYLENE-HEPTYLSELANYL)-BENZENE
• CAS NO: 63831-77-6
• Molecular Formula: C₁₄H₂₀Se
• Molecular Weight: 218.40998
• Mol File: 63831-77-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 317.3±15.0 °C(Predicted)
• Appearance: /
• CAS DataBase Reference: (1-METHYLENE-HEPTYLSELANYL)-BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: (1-METHYLENE-HEPTYLSELANYL)-BENZENE(63831-77-6)
• EPA Substance Registry System: (1-METHYLENE-HEPTYLSELANYL)-BENZENE(63831-77-6)

Safety Data

• Hazardous Substances Data: 63831-77-6(Hazardous Substances Data)

Usage

General Description

(1-Methylene-heptylselanyl)-benzene is a chemical compound with the molecular formula C16H24Se. It is a member of the organoselenium compounds and belongs to the class of benzene derivatives. (1-METHYLENE-HEPTYLSELANYL)-BENZENE contains a benzene ring with a heptylselanyl substitution. Organoselenium compounds are known for their various biological activities and have been investigated for their potential use in medicine and pharmacology. Further research is needed to fully understand the properties and potential applications of (1-methylene-heptylselanyl)-benzene.

Upstream product

• 629-05-0 n-octyne 
• 645-96-5 Benzeneselenol 
• 1666-13-3 diphenyl diselenide 

Downstream Products

• 66717-00-8 2-phenylseleno-2-octene 
• 103971-60-4 2,2-bis(phenylselenyl) octane 

Relevant articles and documents

Highly regioselective hydroselenation and double-bond isomerization of terminal alkynes with benzeneselenol catalyzed by bis(triphenylphosphine) palladium(II) dichloride

Bis(triphenylphosphine)palladium(II) dichloride (PdCl2(PPh 3)2) catalyzes regioselective addition of benzeneselenol to terminal alkynes and the subsequent double-bond isomerization to afford the corresponding internal alkenyl selenides in good yields.

The Pt-Catalyzed Carboselenation of Alkynes by Selenoesters

(Matrix presented) The Pt-catalyzed carboselenation of terminal alkynes with selenoesters provided vinylselenides regio- and stereoselectively in moderate yields.

The first example of transitionmetal-catalyzed hydroselenation of acetylenes

A variety of transition metal complexes catalyzed the regioselective hydroselenation of acetylenes. In particular, the palladium acetate-catalyzed reaction afforded the Markovnikov adducts with high selectivity.