19917-00-1

Basic information

• Product Name: trimethyl[(1-phenylprop-2-en-1-yl)oxy]silane
• CAS NO: 19917-00-1
• Molecular Formula: C₁₂H₁₈OSi
• Molecular Weight: 206.3562
• Mol File: 19917-00-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 237.2°C at 760 mmHg
• Flash Point: 92°C
• Density: 0.912g/cm³
• Vapor Pressure: 0.0697mmHg at 25°C
• Refractive Index: 1.482
• CAS DataBase Reference: trimethyl[(1-phenylprop-2-en-1-yl)oxy]silane(CAS DataBase Reference)
• NIST Chemistry Reference: trimethyl[(1-phenylprop-2-en-1-yl)oxy]silane(19917-00-1)
• EPA Substance Registry System: trimethyl[(1-phenylprop-2-en-1-yl)oxy]silane(19917-00-1)

Safety Data

• Hazardous Substances Data: 19917-00-1(Hazardous Substances Data)

Usage

General Description

Trimethyl[(1-phenylprop-2-en-1-yl)oxy]silane is a chemical compound with the formula C14H21OSi. It is a silane derivative that contains a phenylpropenyl group attached to a silicon atom through an oxygen atom. trimethyl[(1-phenylprop-2-en-1-yl)oxy]silane is commonly used as a silane coupling agent in various industrial applications, particularly in the production of adhesives, sealants, and coatings. It acts as a bonding agent that enhances the adhesion of organic materials to inorganic substrates, such as glass, metal, or ceramics. Trimethyl[(1-phenylprop-2-en-1-yl)oxy]silane is known for its ability to improve the performance and durability of composite materials, as well as its water and UV resistance properties. Additionally, it is considered to be a versatile chemical that finds applications in the fields of plastics, rubber, and construction materials.

Upstream product

• 100-52-7 benzaldehyde 
• 10519-96-7 potassium trimethylsilonate 
• 95932-32-4 tert-butyl (E)-cinnamyl carbonate 
• 75-77-4 chloro-trimethyl-silane 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 593-60-2 Vinyl bromide 
• 123159-55-7 <2-(trimethylsilyl)ethyl>tris(2-methylphenyl)phosphonium iodide 

Downstream Products

• 1083-30-3 dihydrochalcone 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 112741-53-4 (3R,5S,6R)-4-(benzyloxycarbonyl)-5,6-diphenyl-3-(2'-oxo-2'-phenylethyl)-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-one 
• 100516-57-2 (3S,5S,6R)-4-(benzyloxycarbonyl)-5,6-diphenyl-3-(2'-oxo-2'-phenylethyl)-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-one 
• 3412-44-0 (1E)-1,3-diphenylpropene 
• 62056-38-6 (E)-1-phenyl-3-p-tolylpropene 
• 18916-11-5 (E)-1-methyl-2-(3-phenyl-2-propen-1-yl)benzene 
• 20442-73-3 (1E)-3-(4-methoxyphenyl)-1-phenylpropene 
• 20442-73-3 (Z)-1-methoxy-4-(3-phenyl-2-propen-1-yl)benzene 
• 149045-39-6 1-methoxy-2-[(2E)-3-phenyl-2-propen-1-yl]benzene 
• 485844-19-7 1-fluoro-4-[(2E)-3-phenyl-2-propen-1-yl]benzene 
• 57294-86-7 (E)-cinnamyl azide 
• 66323-99-7 trimethyl[(Z)-(1-phenyl-1-propenyl)oxy]silane 
• 71268-59-2 (E)-1-phenyl-1-(trimethylsiloxy)propene 

Relevant articles and documents

Iron-Catalyzed Grignard Cross-Couplings with Allylic Methyl Ethers or Allylic Trimethylsilyl Ethers

We have found that cross-coupling between aryl Grignard reagents and allylic methyl ethers proceeded well in the presence of a catalytic amounts of Fe(acac) 3 to afford the corresponding allylic substitution products in good yields. Under the same conditions, allylic trimethylsilyl ethers also reacted with Grignard reagents to give the corresponding cross-coupling products.

Wittig rearrangement of lithiated allyl aryl ethers: A mechanistic study

At -75°C, α-lithiated allyl phenyl ether undergoes mainly the [1,2] Wittig rearrangement to afford, after acidic hydrolysis, 1-phenyl-2-propen-1-ol as the main product. A second metalation taking place at one of the ortho positions is the sole competing s

Ni/Cr/Al multi-metal redox-mediated alkenylation of aldehydes

Alkenylation of aldehydes mediated by a catalytic amount of Cr(II)/Ni(0), using aluminium as an electron source, was performed to afford the corresponding allyl alcohol derivatives in good to moderate yields.