16664-48-5

Basic information

• Product Name: 6-bromo-1-phenyl-1-hexyne
• Synonyms: 6-bromo-1-phenyl-1-hexyne
• CAS NO: 16664-48-5
• Molecular Weight: 237.139
• Mol File: 16664-48-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 6-bromo-1-phenyl-1-hexyne(CAS DataBase Reference)
• NIST Chemistry Reference: 6-bromo-1-phenyl-1-hexyne(16664-48-5)
• EPA Substance Registry System: 6-bromo-1-phenyl-1-hexyne(16664-48-5)

Safety Data

• Hazardous Substances Data: 16664-48-5(Hazardous Substances Data)

Upstream product

• 69936-53-4 6-phenylhex-5-yn-1-ol 
• 110-52-1 1,4-dibromo-butane 
• 4440-01-1 lithium phenylacetylide 
• 536-74-3 phenylacetylene 

Downstream Products

• 16664-52-1 hex-5-en-1-yn-1-ylbenzene 
• 4410-77-9 benzylidenecyclopentane 
• 15507-35-4 1-benzylcyclopentene 
• 1129-65-3 (hex-1-yn-1-yl)benzene 
• 771-98-2 1-Phenylcyclohexene 
• 6111-82-6 1-phenylhex-1-ene 
• 1188283-99-9 1-(6-phenylhex-5-yn-1-yl)cyclopentan-1-ol 
• 1188284-00-5 1-(6-phenyl-hex-5-ynyl)-cyclobutanol 
• 262594-04-7 6-phenyl-5-hexynylphosphine 
• 376600-19-0 diethyl-6-phenyl-5-hexynylphosphonate 
• 431911-37-4 diethyl (1-phenyl-1-hexyn-6-yl)malonate 
• 1254985-02-8 N-(2,2-diethoxyethyl)-4-methyl-N-(6-phenylhex-5-ynyl)-benzenesulfonamide 
• 1416161-37-9 C₁₉H₂₈S₂Si 
• 126497-27-6 2-cyclopentylidene-1-phenylacetic acid 

Relevant articles and documents

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Metal-Free Synthesis of Highly Substituted Pyridines by Formal [2+2+2] Cycloaddition under Mild Conditions

The synthesis of pyridines through direct intermolecular cycloaddition of alkynes and nitriles is a contemporary challenge in organic synthesis. A Br?nsted acid mediated formal [2+2+2] cycloaddition of heteroalkynes and nitriles was developed that proceed

An unprecedented tandem annulation of ω-azido-1-alkynes with diaryl-iodonium salts: A facile synthesis of polycyclic quinolines

Polysubstituted quinolines are synthesized through an unprecedented cascade annulation of ω-azido-1-alkynes with diaryliodonium salts, which serve as C2-building blocks. The reaction proceeds smoothly and is catalyzed by Cu(I) catalysts to give various qu