67649-77-8

Basic information

• Product Name: Benzene, (1-hexenylseleno)-, (E)-
• CAS NO: 67649-77-8
• Molecular Formula: C12H16Se
• Molecular Weight: 239.219
• Mol File: 67649-77-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, (1-hexenylseleno)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (1-hexenylseleno)-, (E)-(67649-77-8)
• EPA Substance Registry System: Benzene, (1-hexenylseleno)-, (E)-(67649-77-8)

Safety Data

• Hazardous Substances Data: 67649-77-8(Hazardous Substances Data)

Upstream product

• 109-72-8 n-butyllithium 
• 65910-12-5 (phenylselanyl)acetylene 
• 108-86-1 bromobenzene 
• 1119-67-1 1-iodo-1-hexyne 
• 68001-64-9 (hex-1-ynyl)(phenyl)selane 
• 34837-55-3 Phenylselenyl bromide 
• 693-02-7 hex-1-yne 
• 109-65-9 1-bromo-butane 
• 3844-94-8 1-(trimethylsilyl)-1-hexyne 
• 155623-79-3 (E)-1-(phenylseleno)-1-(trimethylsilyl)-1-hexene 
• 5707-04-0 Phenylselenyl chloride 
• 42599-18-8 (E)-1-hexenyldihydroxyborane 

Downstream Products

• 67649-80-3 ((E)-1-Methyl-hex-1-enylselanyl)-benzene 
• 92-52-4 biphenyl 
• 6111-82-6 1-phenylhex-1-ene 
• 7433-56-9 (E)-5-decene 
• 104-51-8 1-butylbenzene 

Relevant articles and documents

Stereoselective synthesis of 1,1-bimetalloalkenes of tin and selenium, tin and tellurium

1,1-Bimetalloalkenes(tin and selenium, tin and tellurium) were stereoselectively prepared by a hydrozirconation of acetylenic stannanes followed by transmetallation using tellurenyl iodide and selenenyl bromide. One equivalent of n-BuLi displaced a trialk

Preparation of (Z)- and (E)-vinyl selenides utilizing vinylboronic acids and vinylboronic esters in ionic liquids

Vinylboronic acids and vinylboronic esters react with phenylselenyl chloride in ionic liquids to generate vinyl selenides stereospecifically.

Vicinal di￡unctionalization of alkynyl selenides with lithium butylcyano cuprate and electrophiles

Alkynyl selenides react with lithium butylcyano cuprate giving an intermediate lithium vinylcyano cuprate, which is trapped with electrophiles to give several classes of vinylic selenides.