13436-82-3 Usage
General Description
But-2-enyltriethoxysilane is a chemical compound that consists of a but-2-enyl group (a type of organic compound containing two carbon atoms in a double bond) and three triethoxysilane groups (a silicon-based compound with three ethoxy groups attached). but-2-enyltriethoxysilane is commonly used as a coupling agent in the production of adhesives, sealants, and coatings, where it can improve adhesion and durability by forming strong bonds between organic and inorganic materials. But-2-enyltriethoxysilane is also utilized as a surface modifier in the production of reinforced polymers and composites, as it can enhance the compatibility between the polymer matrix and the reinforcing filler, leading to improved mechanical properties and performance. Additionally, this compound is known for its ability to improve the water and chemical resistance of various materials, making it a valuable ingredient in the development of durable and long-lasting products.
Check Digit Verification of cas no
The CAS Registry Mumber 13436-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,3 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13436-82:
(7*1)+(6*3)+(5*4)+(4*3)+(3*6)+(2*8)+(1*2)=93
93 % 10 = 3
So 13436-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O3Si/c1-5-9-10-14(11-6-2,12-7-3)13-8-4/h5,9H,6-8,10H2,1-4H3/b9-5+
13436-82-3Relevant articles and documents
1,2-selective hydrosilylation of conjugated dienes
Parker, Sarah E.,B?rgel, Jonas,Ritter, Tobias
, p. 4857 - 4860 (2014)
Selective 1,2-hydrosilylation of 1,3-dienes is a challenging problem in transition metal catalysis. Butadiene, specifically, would be a useful substrate because 3-butenylsilane products have promise as superior coupling reagents for hybrid organic/inorganic materials synthesis. We report the first selective 1,2-hydrosilylation of conjugated dienes including butadiene. Hydrosilylation proceeds through a Pt(II/IV) cycle, and selectivity is generated at a hexacoordinate Pt(IV) complex that favors 2-diene coordination and prevents π-allyl complex formation.