129758-71-0

Usage

Uses

Used in Biodegradable Plastics Industry:
3-Hydroxyundecanoic acid methyl ester is used as a monomer for the production of biodegradable plastics. Its unique structure allows for the creation of polymers with desirable properties, such as biodegradability and biocompatibility, making it an environmentally friendly alternative to traditional petroleum-based plastics.
Used in Pharmaceutical Industry:
3-Hydroxyundecanoic acid methyl ester is used as an intermediate in the synthesis of various pharmaceutical compounds. Its versatile chemical structure enables the development of new drugs with potential applications in treating various medical conditions.
Used in Cosmetics Industry:
3-Hydroxyundecanoic acid methyl ester is used as an ingredient in the formulation of cosmetics and personal care products. Its unique properties, such as emollient and moisturizing effects, make it a valuable component in creating products with improved skin feel and appearance.
Used in Lubricants Industry:
3-Hydroxyundecanoic acid methyl ester is used as a component in the formulation of lubricants. Its ability to form stable esters and its compatibility with various base oils make it a suitable candidate for use in the development of high-performance lubricants with improved tribological properties.
Used in Fuel Industry:
3-Hydroxyundecanoic acid methyl ester is used as a potential biofuel component. Its properties, such as high energy density and low toxicity, make it a promising candidate for blending with conventional fuels to create more sustainable and environmentally friendly energy sources.

Upstream product

• 124-19-6 nonan-1-al 
• 36850-80-3 [(1-methoxyvinyl)oxy]trimethylsilane 
• 22104-71-8 methyl undec-2-enoate 
• 133842-22-5 C₁₈H₃₈O₄Si 
• 2404-44-6 1,2-Epoxydecane 
• 67-56-1 methanol 
• 120703-51-7 1-Methoxy-1,1-bis-trimethylsilanyl-undecan-3-ol 

Relevant academic research and scientific papers

An environmentally friendly procedure for Mukaiyama aldol and Mukaiyama-Michael reactions using a catalytic amount of DBU under solvent- and metal-free conditions

Mukaiyama aldol and Mukaiyama-Michael reactions can proceed smoothly in the presence of a catalytic amount of DBU (20% mmol), to afford the corresponding products in moderate to good yields. This solvent- and metal-free approach provides an environmentall

New one carbon homologation reagents utilizing electrochemical oxidation of organosilicon compounds

Phenylthio(trimethylsilyl)methane, phenylthiobis(trimethylsilyl)methane, methoxy(trimethylsilyl)-methane, and methoxybis(trimethylsilyl)methane are deprotonated and the resulting anions are alkylated with electrophiles such as organic halides. The alkylation products are readily converted into the corresponding dimethyl acetals or methyl esters by electrochemical oxidation in methanol.

An Efficient Method for the Direct Peroxygenation of Various Olefinic Compounds with Molecular Oxygen and Triethylsilane Catalyzed by a Cobalt(II) Complex

An efficient method for the direct peroxygenation of various olefinic compounds with molecular oxygen and triethylsilane (Et3SiH) was developed by the use of a catalytic amount of a bis(1,3-diketonato)cobalt(II) complex.According to the above method, 1-phenyl-3-triethylsilyldioxybutane (2) was directly produced from 4-phenyl-1-butene (1) by means of a reaction with O2 and Et3SiH at room temperature.Styrene (3) and ethyl acrylate (5a) were also smoothly peroxygenated to give 1-phenyl-1-triethylsilyldioxyethane (4) and ethyl 2-triethylsilyldioxypropionate (6a) by using a small amount of t-BuOOH as an initiator.The successive desilylation of 6a and reduction of the resulting ethyl 2-hydroperoxypropionate (8a) afforded the corresponding alcohol, ethyl lactate (10a), in a high yield.The synthetic utility of the present peroxygenation reaction was demonstrated in the preparation of α-hydroxy esters 10a-e from several α,β-unsaturated esters 5a-e via the corresponding triethylsilyldioxy derivatives.

METHOXY(TRIMETHYLSILYL)METHANE AND METHOXYBIS(TRIMETHYLSILYL)METHANE AS NEW REAGENTS FOR HOMOLOGATION

New synthons of formyl anion methoxy(trimethylsilyl)methane (1)) and alkoxycarbonyl anion (methoxybis(trimethylsilyl)methane (2)) have been developed using oxidative cleavage of the carbon-silicon bond by anodic oxidation.