10508-66-4

Basic information

• Product Name: 1-Phenyl-1,3-hexadiyne
• Synonyms: 1-Phenyl-1,3-hexadiyne;Neocapillene
• CAS NO: 10508-66-4
• Molecular Formula: C₁₂H₁₀
• Molecular Weight: 0
• Mol File: 10508-66-4.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Phenyl-1,3-hexadiyne(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Phenyl-1,3-hexadiyne(10508-66-4)
• EPA Substance Registry System: 1-Phenyl-1,3-hexadiyne(10508-66-4)

Safety Data

• Hazardous Substances Data: 10508-66-4(Hazardous Substances Data)

Usage

Type of compound

Alkyne

Presence of bonds

Carbon-carbon triple bonds

Usage

Building block for the synthesis of various aromatic compounds

Physical state

Colorless liquid at room temperature

Flammability

Highly flammable

Applications

Production of polymers, pharmaceuticals, and agrochemicals

Importance

Valuable tool for researchers and scientists in organic chemistry

Upstream product

• 50405-39-5 1-bromobut-1-yne 
• 536-74-3 phenylacetylene 
• 879560-02-8 (1,1-dibromobut-1-en-3-yn-2-yl)benzene 
• 75-03-6 ethyl iodide 
• 36038-37-6 3,4,4,4-Tetrachlor-1-phenyl-1-butin 
• 6181-26-6 1-trichloromethyl-3-phenyl-2-propyn-1-ol 
• 591-50-4 iodobenzene 
• 10508-63-1 1-phenylhex-2-yne-1,4-diol 
• 36038-38-7 1,1,2-Trichlor-4-phenyl-1-buten-3-in 
• 74-96-4 ethyl bromide 
• 81588-19-4 1-ethylthio-4-phenyl-1-buten-3-yne 

Relevant articles and documents

One-pot synthesis and functionalization of polyynes via alkylidene carbenoids

A one-pot, two-step method for the synthesis of diynes and triynes is reported. The reaction of a dibromoolefinic precursor with BuLi effects a Fritsch-Buttenberg-Wiechell rearrangement and generates a lithium acetylide intermediate, which is then trapped

A new procedure for the synthesis of aryl- or hetaryl-substituted conjugated diynes

On treatment with two equivalents of NaNH2 in liquid ammonia the enyne sulfides RCC-CH=CHSEt (cis-isomers, where R is an aryl or a hetaryl) affords sodium salts of 1,3-diynes.The latter react with ethyl bromide to produce disubstituted diynes RCC-C