Phenyltrimethylsilane

• CAS: 768-32-1
• Catalog Number: ACM768321
• Category: Alkyl Silane
• Molecular Weight: 150.3 g/mol
• Molecular Formula: C9H14Si
• Synonyms: Trimethylphenylsilane
• IUPAC Name: trimethyl(phenyl)silane
• Canonical SMILES: C[Si](C)(C)C1=CC=CC=C1
• InChI Key: KXFSUVJPEQYUGN-UHFFFAOYSA-N
• Boiling Point: 169-170 °C
• Flash Point: 40 °C
• Density: 0.873 g/mL
• Appearance: Liquid
• Storage: Ambient temperatures.
• EC Number: 212-192-5
• Exact Mass: 150.08600
• Hazard Statements: H226; H318; H413
• Packaging: 10 g; 100 g
• Packing Group: III
• Precautionary Statements: P210; P233; P240; P241; P242; P243; P273; P280; P303+P361+P353; P305+P351+P338; P310; P370+P378; P403+P235; P501
• Safety Description: S16-S26-S37/39
• Signal Word: Danger
• WGK Germany: 3

Custom Q&A

What is the molecular formula of Phenyltrimethylsilane?

The molecular formula of Phenyltrimethylsilane is C9H14Si.

What are some synonyms for Phenyltrimethylsilane?

Some synonyms for Phenyltrimethylsilane include trimethyl(phenyl)silane, 768-32-1, Trimethylphenylsilane, and Silane, trimethylphenyl.

What is the molecular weight of Phenyltrimethylsilane?

The molecular weight of Phenyltrimethylsilane is 150.29 g/mol.

What is the IUPAC name of Phenyltrimethylsilane?

The IUPAC name of Phenyltrimethylsilane is trimethyl(phenyl)silane.

What is the InChIKey of Phenyltrimethylsilane?

The InChIKey of Phenyltrimethylsilane is KXFSUVJPEQYUGN-UHFFFAOYSA-N.

How many hydrogen bond donor counts does Phenyltrimethylsilane have?

Phenyltrimethylsilane has 0 hydrogen bond donor counts.

How many hydrogen bond acceptor counts does Phenyltrimethylsilane have?

Phenyltrimethylsilane has 0 hydrogen bond acceptor counts.

What is the topological polar surface area of Phenyltrimethylsilane?

The topological polar surface area of Phenyltrimethylsilane is 0 Ų.

How many rotatable bond counts does Phenyltrimethylsilane have?

Phenyltrimethylsilane has 1 rotatable bond count.

Is the compound canonicalized?

Yes, the compound is canonicalized.

Synthetic Use

Upstream Synthesis Route 1

• 75-77-4
• 603-35-0

• 768-32-1
• 17154-34-6

Reference: [1] Journal of Organic Chemistry, 1987, vol. 52, # 5, p. 748 - 753
[2] Journal of Organic Chemistry, 1987, vol. 52, # 5, p. 748 - 753

Upstream Synthesis Route 2

• 18090-43-2

• 768-32-1
• 13183-70-5
• 2060-89-1

Reference: [1] Chemistry Letters, 1983, p. 599 - 602
[2] Journal of the American Chemical Society, 1983, vol. 105, # 21, p. 6436 - 6442

Upstream Synthesis Route 3

• 75-77-4
• 108-90-7

• 768-32-1

Reference: [1]Current Patent Assignee: WUHAN UNIVERSITY - CN113072575, 2021, A
Location in patent: Paragraph 0029-0043

Downstream Synthesis Route 1

• 1003-09-4
• 768-32-1

• 29488-24-2

Reference: [1] Journal of the American Chemical Society, 2014, vol. 136, # 1, p. 254 - 264

Downstream Synthesis Route 2

• 768-32-1

• 16029-98-4

Reference: [1]Eaborn, C.
[Journal of the Chemical Society][Journal of the Chemical Society, 1950, p. 3077 - 3089]
[Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Si: MVol.C, 64, page 179 - 181]
[2]Pray et al.
[Journal of the American Chemical Society, 1948, vol. 70, p. 433]
[Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Si: MVol.C, 64, page 179 - 181]
[3]Eaborn
[Journal of the Chemical Society, 1950, p. 3077,3084]
[4]Pray et al.
[Journal of the American Chemical Society, 1948, vol. 70, p. 433]

Downstream Synthesis Route 3

• 768-32-1

• 10151-74-3

Reference: [1]Daniels, Rhys G.; Paquette, Leo A.
[Journal of Organic Chemistry, 1981, vol. 46, # 14, p. 2901 - 2910]
[2]Wiesenfeldt, Mario P.; Knecht, Tobias; Schlepphorst, Christoph; Glorius, Frank
[Angewandte Chemie - International Edition, 2018, vol. 57, # 27, p. 8297 - 8300][Angew. Chem., 2018, vol. 130, # 27, p. 8429 - 8432,4]
[3]Gelis, Coralie; Heusler, Arne; Nairoukh, Zackaria; Glorius, Frank
[Chemistry - A European Journal, 2020, vol. 26, # 62, p. 14090 - 14094]
[4]Kanazashi; Takakusa
[Bulletin of the Chemical Society of Japan, 1954, vol. 27, p. 441,443]

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