26306-00-3

Usage

Uses

Used in Organic Synthesis:
[(6-Bromohexyl)oxy]trimethylsilane is used as a reagent in the field of organic synthesis for its ability to facilitate various chemical reactions and transformations, contributing to the creation of a multitude of organic compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, [(6-Bromohexyl)oxy]trimethylsilane is utilized as a key building block in the synthesis of bioactive molecules, playing a crucial role in the development of new drugs and therapeutic agents.
Used in Agrochemicals:
This organosilicon compound is also employed in the production of agrochemicals, where it serves as an essential component in the synthesis of various chemical products used in agriculture.
Used in the Construction of Siloxane-based Materials:
[(6-Bromohexyl)oxy]trimethylsilane is used as a fundamental component in the construction of functionalized siloxane-based materials, which have a wide range of applications in the industry due to their unique properties.
Used as a Protecting Group for Alcohols:
In organic chemistry, [(6-Bromohexyl)oxy]trimethylsilane is used as a protecting group for alcohols, safeguarding them from unwanted reactions during the synthesis process, and allowing for selective deprotection when needed.

Upstream product

• 4286-55-9 1-bromo-6-hexanol 
• 4224-70-8 6-bromohexanoic acid 
• 75-77-4 chloro-trimethyl-silane 
• 10416-59-8 N,O-bis-(trimethylsilyl)-acetamide 

Downstream Products

• 114423-59-5 3-<6'-(trimethylsilyloxy)hexyl>-1-<(trimethylsilyl)oxy>cyclohexene 
• 35148-19-7 (E)-9-dodecenyl acetate 
• 1438243-35-6 C₂₁H₄₄B₁₀OSi 
• 114489-14-4 trans,trans-(5S)-5-<9'-(2,3-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-3-methylenetetrahydro-2-furanone 
• 114423-67-5 trans,trans-5-<9'-(2'',3''-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-3-methylenetetrahydro-2-furanone 
• 114489-16-6 trans,trans-(5S)-5-<9'-(2,3-dihydroxycyclohexyl)-3'-nonenyl>-3-methylenetetrahydro-2-furanone 
• 114423-68-6 trans,trans-5-<9'-(2'',3''-dihydroxycyclohexyl)-3'-nonenyl>-3-methylenetetrahydro-2-furanone 
• 114423-63-1 <6'-(trans,trans-1'',2''-bis((dimethylthexylsilyl)oxy)-3''-cyclohexyl)hexyl>triphenylphosphonium bromide 
• 114528-96-0 trans,trans-(5S)-5-<9'-(2,3-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-2,3-dihydrofuranone 
• 114423-64-2 trans,trans-3-(10'-acetoxy-6'-decenyl)-1,2-bis<(dimethylthexylsilyl)oxy>cyclohexane 
• 114423-66-4 trans,trans-3-(10'-oxo-6'-decenyl)-1,2-bis<(dimethylthexylsilyl)oxy>cyclohexane 
• 114423-65-3 trans,trans-3-(10'-hydroxy-6'-decenyl)-1,2-biscyclohexane 
• 114423-62-0 trans,trans-3-(6'-bromohexyl)-1,2-bis<(dimethylthexylsilyl)oxy>cyclohexane 
• 114423-61-9 trans,trans-3-(6'-bromohexyl)-1,2-cyclohexanediol 

Relevant academic research and scientific papers

Exo and endohormones. XX. Synthesis of racemic 2-ethyl-1,6-dioxaspiro[4,4]nonane, the aggregation pheromone of pityogenes chalcographus (Coleoptera, Scolytidae)

The synthesis of a diastereoisomeric mixture of 2-etyl-1,6-dioxaspiro[4,4]nonane (chalcograne) a main component of the aggregation pheromone of the spruce bark beetle Pityogenes chalcographus (Coleoptera, Scolytidae), a serious pest in European forests, by 1,7-nonanediol cyclization using Pb(OAc)4 is given below. The side products of spirocyclization were identified by GC/MS.

Synthesis of a Model Hapten with Cyclohexanediol and &α-Methylene-&γ-butyrolactone Groups, a Synthetic Analogue of Poison Ivy and Tulipalin Allergens Connected with a Carbon Chain

Potential skin sensitizers 1 and 1* with two different haptenic ends, (a) a cyclohexanediol group (saturated poison ivy analogue ) and (b) an α-methylene-γ-butyrolactone moiety (tulipalin A), separated by a nine carbon atoms chain containing a double bond have been prepared.The trans, trans relationship in the substituted cyclohexanediol was secured by a tandem Michael addition-hydroboration reaction.Contrary to an earlier example of a double-headed hapten containing pyrocatechol and α-methylene-γ-butyrolactone ends, the cyclohexanediol-α-methylene-γ-butyrolactone does not show any tolerance induction to the α-methylene-γ-butyrolactone end.It therefore seems that induction of tolerance as well as sensitization requires the formation of covalent bond with a protein carrier.

Synthesis of codling moth attractant

Sterospecific synthesis of an attractant for the codling moth by reacting sorbic aldehyde with an organo-metallic reagent to yield a 1-ether of trans-8-trans-10-dodecadiene-1,7-diol which is reduced via a 7-sulfonic acid ester to yield an ether of trans-8-trans-10-dodecadiene-1-ol and hydrolyzed to trans-8-trans-10-dodecadien-1-ol. SPC1