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26306-02-5

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26306-02-5 Usage

Description

[(10-bromodecyl)oxy]trimethylsilane is a chemical compound that features a trimethylsilyl group and a 10-bromodecyl group connected by an oxygen atom. [(10-bromodecyl)oxy]trimethylsilane is known for its utility in organic synthesis, particularly in the modification of surfaces and polymers. The trimethylsilyl group serves as a protective group for alcohols and carboxylic acids, while the 10-bromodecyl group contributes hydrophobic properties to materials.

Uses

Used in Organic Synthesis:
[(10-bromodecyl)oxy]trimethylsilane is used as a reagent for the modification of surfaces and polymers, enhancing their properties and performance in various applications.
Used in Surface Modification:
[(10-bromodecyl)oxy]trimethylsilane is used as a surface modifier to introduce hydrophobic properties to different materials, which can be beneficial in various industries such as coatings, adhesives, and textiles.
Used in the Production of Functionalized Silicon Materials:
[(10-bromodecyl)oxy]trimethylsilane is utilized as a key component in the synthesis of functionalized silicon materials, which have a wide range of applications in the electronics, automotive, and aerospace industries.
Used in Silica Surface Modification:
[(10-bromodecyl)oxy]trimethylsilane is also employed in modifying silica surfaces for applications in materials science and technology, where improved surface properties can lead to enhanced performance and functionality.
Used in Coatings Industry:
[(10-bromodecyl)oxy]trimethylsilane is used as an additive to impart hydrophobic properties to coatings, making them more resistant to water, stains, and other environmental factors.
Used in Adhesives Industry:
In the adhesives industry, this compound is used to modify the properties of adhesives, providing better adhesion and durability on various surfaces.
Used in Textile Industry:
[(10-bromodecyl)oxy]trimethylsilane is used to introduce hydrophobic and oleophobic properties to textiles, making them more resistant to water and oil-based stains, and improving their overall performance.

Check Digit Verification of cas no

The CAS Registry Mumber 26306-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,3,0 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26306-02:
(7*2)+(6*6)+(5*3)+(4*0)+(3*6)+(2*0)+(1*2)=85
85 % 10 = 5
So 26306-02-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H29BrOSi/c1-16(2,3)15-13-11-9-7-5-4-6-8-10-12-14/h4-13H2,1-3H3

26306-02-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(10-bromodecyl)oxy]trimethylsilane

1.2 Other means of identification

Product number -
Other names 10-BROMODECYL TRIMETHYLSILYL ETHER

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26306-02-5 SDS

26306-02-5Downstream Products

26306-02-5Relevant articles and documents

Synthesis principle and processing process of chilo suppressalis and tryporyza incertulas pheromone

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Paragraph 0014, (2018/09/11)

The invention relates to synthesis principle of chilo suppressalis and tryporyza incertulas pheromone. The synthesis principle comprises the following operation steps of A, preparing monoprotection tridecane diol; performing manufacturing by using 1,10-decanediol, 3-bromopropyl alcohol and amyltriphenylphosphonium bromide as raw materials; B, oxidizing the monoprotection tridecane diol into aldehyde; C, constructing 13-site cis-double bonds through wittig reaction to complete 13Z-18OH preparation. The raw materials are cheap and can be easily obtained; all reaction types can easily realize industrial production; the coarse product purity is high; the purification is easy; the process has high selectivity (Z:E is greater than 14:1); the reaction is simple; the operation is easy; the amplification is easy; the yield is high; the environment pollution is small; the popularization application has good economic and social benefits.

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