71789-10-1

Usage

Uses

Used in Organic Chemistry Research:
1-Trimethylsilyl-1,4-pentadiyne is used as a synthetic building block for the creation of complex organic molecules, facilitating various chemical reactions such as cross-coupling and cycloaddition. Its presence in research laboratories is due to its ability to contribute to the development of new organic compounds and materials.
Used in Industrial Settings:
In the chemical industry, 1-Trimethylsilyl-1,4-pentadiyne is used as a reagent in the synthesis of a wide range of products, including pharmaceuticals, agrochemicals, and specialty chemicals. Its versatility in facilitating multiple types of reactions makes it a valuable component in industrial chemical processes.
Used in Safety and Handling Protocols:
Due to its high reactivity and flammability, 1-Trimethylsilyl-1,4-pentadiyne is also used as a subject in the development of safety and handling protocols within laboratories and industrial environments. This ensures that professionals can work with the compound safely and effectively, minimizing risks associated with its use.

InChI:InChI=1/C8H12Si/c1-5-6-7-8-9(2,3)4/h1H,6H2,2-4H3

Upstream product

• 6165-76-0 propargyl p-toluenesulfonate 
• 61210-52-4 (trimethylsilyl)ethynylmagnesium bromide 
• 593-61-3 bromoethyne 
• 106-96-7 propargyl bromide 
• 1066-54-2 trimethylsilylacetylene 

Downstream Products

• 853929-57-4 Benzoic acid (E)-(S)-1-((Z)-pent-2-enyl)-8-trimethylsilanyl-oct-2-ene-4,7-diynyl ester 
• 403696-87-7 2-((E)-(S)-1-Hydroxy-3-methyl-hexa-2,5-dienyl)-4-methoxy-5-((Z)-2-methyl-hept-2-en-6-ynyl)-phenol 
• 403696-86-6 2-((E)-(S)-1-Hydroxy-3-methyl-hexa-2,5-dienyl)-4-methoxy-5-((Z)-2-methyl-7-triisopropylsilanyl-hept-2-en-6-ynyl)-phenol 
• 403696-85-5 2-((E)-(S)-1-Hydroxy-3-methyl-hex-2-en-5-ynyl)-4-methoxy-5-((Z)-2-methyl-7-triisopropylsilanyl-hept-2-en-6-ynyl)-phenol 
• 403696-77-5 1-(tert-butyl-dimethyl-silanyloxy)-2-[1-(tert-butyl-dimethyl-silanyloxy)-3-methyl-hexa-2,5-dienyl]-4-methoxy-5-(2-methyl-hept-2-en-6-ynyl)-benzene 
• 403696-84-4 (E)-(S)-1-[2-(tert-Butyl-dimethyl-silanyloxy)-5-methoxy-4-((Z)-2-methyl-7-triisopropylsilanyl-hept-2-en-6-ynyl)-phenyl]-3-methyl-6-trimethylsilanyl-hex-2-en-5-yn-1-ol 
• 591253-85-9 (5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[4-(3-(trimethylsilyl)-2-propynyl)-1,2,3-triazol-1-ylmethyl]oxazolidin-2-one 
• 321165-47-3 Ru2(μ-NCPh2)(μ-η(2)-CH2CCH2CCSiMe3)(CO)6 
• 1262768-99-9 B 064-055A₁ 
• 1433554-90-5 1-benzyloxycarbonylmethyl-4-[3-(trimethylsilyl)prop-2-ynyl]-1H-1,2,3-triazole 
• 1433554-91-6 1-[2-(benzyloxycarbonyl)-2-propyl]-4-[3-(trimethylsilyl)prop-2-ynyl]-1H-1,3,3-triazole 
• 78037-99-7 (5S)-(6E,8Z,11Z,14Z)-5-hydroxy-eicosa-6,8,11,14-tetraenoic acid, methyl ester 
• 61641-47-2 5(S)-HETE 

Relevant academic research and scientific papers

Electrophilic Aromatic Substitution Reactions of Arsabenzene

Arsabenzene undergoes electrophilic substitution at the 2- and 4-positions.Proton-deuterium exchange takes place in trifluoroacetic acid-d.Friedel-Crafts acetylation and nitration give mixtures of 2- and 4-substituted products. 2- and 4-(trimethylsilyl)arsabenzenes are protodesilylated in trifluoroacetic acid.