Phenyltrimethoxysilane

• CAS: 2996-92-1
• Catalog Number: ACM2996921
• Category: Micro/NanoElectronics
• Molecular Weight: 198.29
• Molecular Formula: C9H14O3Si
• Description: Phenyl-functional silanes can improve the thermal stability of other silanes. Phenyl functional silanes can be used as intermediates for other silanes and siloxanes. Phenyl functional silane can be used for hydrophobic surface treatment. Phenyl functional silanes can be used as hydrophobic additives for other silane coupling agents.
• Synonyms: Benzene, (trimethoxysilyl)-, homopolymer
• IUPAC Name: Trimethoxy(phenyl)silane
• Canonical SMILES: CO[Si](C1=CC=CC=C1)(OC)OC
• InChI: InChI=1S/C9H14O3Si/c1-10-13(11-2,12-3)9-7-5-4-6-8-9/h4-8H,1-3H3
• InChI Key: ZNOCGWVLWPVKAO-UHFFFAOYSA-N
• Boiling Point: 233 °C
• Melting Point: -25 °C
• Flash Point: 99 °F
• Density: 1.062 g/mL at 25 °C (lit.)
• Appearance: Colorless liquid
• Application: It can be used as other silanes and siloxanes intermediates and for hydrophobic surface treatment ,as hydrophobic additive to other silane coupling agents.
• Storage: Inert atmosphere,2- 8 °C
• Complexity: 134
• EC Number: 221-066-9
• Exact Mass: 198.07122084
• Heavy Atom Count: 13
• Monoisotopic Mass: 198.07122084
• Packaging: 10 g; 100 g
• Refractive Index: 1.4680±0.0050
• Specific Gravity: 1.062-1.072
• Topological Polar Surface Area: 27.7 Ų

Custom Reviews

2024-8-30

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Phenyltrimethoxysilane: A Game-Changer in Nanoelectronics and Material Science
As a researcher in material science, using phenyltrimethoxysilane has revolutionized my work. From serving as a crosslinking agent for silicone resin to facilitating the removal of graphene after CVD, this organosilicate compound has proven to be indispensable in my experiments. The ability to synthesize molecularly imprinted sol gels for LSPR fabrication has opened up a world of possibilities for my research. Thank you, Alfa Chemistry, for this amazing product.

Synthetic Use

Downstream Synthesis Route 1

• 1450-85-7
• 2996-92-1

• 7431-45-0

Reference: [1] Journal of Organic Chemistry, 2009, vol. 74, # 14, p. 5118 - 5121

Downstream Synthesis Route 2

• 288-88-0
• 2996-92-1

• 13423-60-4

Reference: [1] Tetrahedron Letters, 2007, vol. 48, # 44, p. 7845 - 7848

Downstream Synthesis Route 3

• 1453-82-3
• 2996-92-1

• 3034-31-9

Reference: [1] Tetrahedron Letters, 2001, vol. 42, # 13, p. 2427 - 2429

Downstream Synthesis Route 4

• 122-20-3
• 2996-92-1

• 54824-83-8

Reference: [1]Journal of Organometallic Chemistry,1975,vol. 85,p. 35 - 39

Downstream Synthesis Route 5

• 150-25-4
• 2996-92-1

• 53883-47-9

Reference: [1]Journal of Organometallic Chemistry,1975,vol. 88,p. 157 - 164

Downstream Synthesis Route 6

• 624-31-7
• 2996-92-1

• 613-33-2
• 644-08-6

Reference: [1]Journal of Organic Chemistry,1999,vol. 64,p. 1684 - 1688
[2]Journal of Organic Chemistry,1999,vol. 64,p. 1684 - 1688

* For details of the synthesis route, please refer to the original source to ensure accuracy.