144192-95-0

Upstream product

• 144192-98-3 1-{[Dimethyl-(1,1,2-trimethyl-propyl)-silanyl]-ethynyl}-2-trimethylsilanylethynyl-benzene 

Downstream Products

• 731857-25-3 1,5-bis{2-[(dimethylthexylsilyl)ethynyl]phenyl}ethynyl-2,4-dibromobenzene 
• 731857-17-3 1,4-bis{2-[(dimethylthexylsilyl)ethynyl]phenyl}ethynyl-2,5-dibromobenzene 
• 731857-27-5 1,5-bis(2-ethynylphenyl)ethynyl-2,4-diethynylbenzene 
• 731857-20-8 1,4-bis(2-ethynylphenyl)ethynyl-2,5-diethynylbenzene 
• 731857-21-9 1,4-bis{2-[(dimethylthexylsilyl)ethynyl]phenyl}ethynyl-2,5-bis(trimethylsilylethynyl)benzene 
• 731857-28-6 1,5-bis{2-[(dimethylthexylsilyl)ethynyl]phenyl}ethynyl-2,4-bis(trimethylsilylethynyl)benzene 
• 223650-64-4 1,2,3-Triethynyl-4-(2-ethynyl-phenylethynyl)-benzene 
• 223650-66-6 2,3-Diethynyl-1,4-bis-(2-ethynyl-phenylethynyl)-benzene 
• 223650-62-2 2-(2-{[dimethyl-(1,1,2-trimethyl-propyl)-silanyl]-ethynyl}-phenylethynyl)-1-trimethylsilanylethynyl-biphenylene 
• 223650-68-8 1,4-Bis-(2-ethynyl-phenylethynyl)-2,3-di-pent-1-ynyl-benzene 
• 1146214-92-7 C₃₀H₂₉BrSi 
• 434343-53-0 2-ethynyl-3-(2-ethynyl-phenylethynyl)-biphenylene 
• 496067-19-7 1,4-Bis-{[dimethyl-(1,1,2-trimethyl-propyl)-silanyl]-ethynyl}-2-(2-{[dimethyl-(1,1,2-trimethyl-propyl)-silanyl]-ethynyl}-phenylethynyl)-3-iodo-benzene 
• 496067-21-1 1-[3,6-diethynyl-2-(2-ethynyl-phenylethynyl)-phenylethynyl]-2-ethynyl-biphenylene 

Relevant academic research and scientific papers

Cobalt-Mediated Synthesis of Angular [4]Phenylene: Structural Characterization of a Metallacyclopentadiene(Alkyne) Intermediate and Its Thermal and Photochemical Conversion

(Matrix Presented) The first X-ray crystal structure of a mononuclear metallacyclopentadiene(alkyne) complex has been obtained. This type of metallacycle is believed to be the key intermediate in the cobalt-mediated [2 + 2 + 2]cycloaddition of alkynes. Th

Synthetic Studies Related to the Esperamicin/Calicheamicin Aglycone: Efficient Construction of a Homochiral Oxabicyclo Analogue from D-Xylose

The synthesis of a bicyclic model of the calicheamicin/esperamicin aglycone is described using a highly efficient and stereospecific Nozaki-Kishi reaction for the ring closure.