92078-65-4

Basic information

• Product Name: (7-bromohept-1-yn-1-yl)benzene
• Synonyms: (7-bromohept-1-yn-1-yl)benzene
• CAS NO: 92078-65-4
• Molecular Weight: 251.166
• Mol File: 92078-65-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (7-bromohept-1-yn-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (7-bromohept-1-yn-1-yl)benzene(92078-65-4)
• EPA Substance Registry System: (7-bromohept-1-yn-1-yl)benzene(92078-65-4)

Safety Data

• Hazardous Substances Data: 92078-65-4(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 34626-51-2 5-bromopentan-1-ol 
• 103935-50-8 5-bromopentyl trifluoromethanesulfonate 
• 111-24-0 1,5-dibromo-pentane 
• 4440-01-1 lithium phenylacetylide 

Downstream Products

• 1311380-61-6 C₂₂H₂₀ClNO 
• 1311380-62-7 C₂₂H₂₀BrNO 
• 154188-72-4 7-phenylhept-6-yn-1-amine 
• 14374-45-9 1-heptynylbenzene 
• 1608-31-7 (cyclohexylidenemethyl)benzene 
• 19016-85-4 hept-6-en-1-ynylbenzene 
• 154188-77-9 2-(7-Phenyl-hept-6-ynyl)-isoindole-1,3-dione 
• 1454697-98-3 9-phenylnon-8-ynenitrile 
• 1454697-37-0 5-fluoro-9-phenyl-1,2,3,4-tetrahydroacridine 
• 1454697-35-8 9-phenyl-7-(trifluoromethyl)-1,2,3,4-tetrahydroacridine 
• 1256344-76-9 2-bromo-9-phenyl-5,6,7,8-tetrahydroacridine 
• 116690-69-8 6-chloro-10-phenyl-1,2,3,4-tetrahydroacridine 
• 1454697-39-2 7-fluoro-9-phenyl-1,2,3,4-tetrahydroacridine 
• 585510-17-4 7-methyl-9-phenyl-1,2,3,4-tetrahydroacridine 

Relevant articles and documents

N-Heterocyclic carbene copper-catalyzed direct alkylation of terminal alkynes with non-activated alkyl triflates

(NHC)-Cu-catalyzed C(sp)-C(sp3) bond formation has been successfully achieved under mild conditions. Nonactivated alkyl triflates, which could be easily derived from alcohols, were utilized as C-O electrophiles. Mechanistic studies suggested th

Rhodium-catalyzed intramolecular cascade sequence for the formation of fused carbazole-annulated medium-sized rings by cleavage of C(sp2)-H/C(sp3)-H bonds

The rhodium(iii)-catalyzed intramolecular annulation of alkyne-tethered 3-(indol-3-yl)-3-oxopropanenitriles for the synthesis of fused carbazole scaffolds via C-H activation has been developed. A series of six-, seven-, and eight-membered hydroazepino[3,2

A concise construction of polycyclic quinolines via annulation of ω-cyano-1-alkynes with diaryliodonium salts

A concise construction of polycyclic quinolines via intramolecular [2 + 2 + 2] annulation of ω-cyano-1-alkynes with diaryliodonium salts was realized. The process produced polycyclic quinolines in high yields with readily available staring materials and was tolerated with halogen substituents.