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Silane, triethyl[(2-methyl-1-propenyl)oxy]-, also known as triethoxy(2-methyl-1-propenyl)silane, is an organosilicon compound with the chemical formula C9H22O2Si. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 194.36 g/mol. Silane, triethyl[(2-methyl-1-propenyl)oxy]- is primarily used as a coupling agent in the production of composite materials, particularly in the reinforcement of plastics and rubber with fillers such as glass fibers. It functions by forming a strong bond between the inorganic filler and the organic matrix, enhancing the mechanical properties and durability of the final product. Additionally, it may be used as a cross-linking agent in the synthesis of silicone polymers and as a reagent in organic synthesis. Due to its reactivity with moisture, it is typically handled under an inert atmosphere and stored away from water and other reactive substances.

7031-16-5

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7031-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7031-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,3 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7031-16:
(6*7)+(5*0)+(4*3)+(3*1)+(2*1)+(1*6)=65
65 % 10 = 5
So 7031-16-5 is a valid CAS Registry Number.

7031-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl (β,β-dimethylvinylhydroxy)silane

1.2 Other means of identification

Product number -
Other names 1-triethylsiloxy-2-methyl-1-propene

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:7031-16-5 SDS

7031-16-5Downstream Products

7031-16-5Relevant academic research and scientific papers

The mechanism of the formation of silyl enol ethers from hydrosilanes and organic carbonyl compounds in the presence of cobalt carbonyls. Kinetic investigation of some reaction steps

Kovács, István,Sisak, Attila,Ungváry, Ferenc,Markó, László

, p. 1025 - 1028 (2008/10/08)

The cleavage of isobutyrylcobalt tetracarbonyl with triethylsilane gives (triethylsilyl)cobalt tetracarbonyl, isobutyraldehyde, dicobalt octacarbonyl, and the corresponding unsaturated and saturated silyl ethers. Silyl enol ether was also formed, along wi

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