4-Fluorophenyltrimethylsilane

• CAS: 455-17-4
• Catalog Number: ACM455174
• Category: Alkyl Silane
• Molecular Weight: 168.28 g/mol
• Molecular Formula: C9H13FSi
• Synonyms: Silane,(4-fluorophenyl)trimethyl-, MolPort-003-933-943, Silane, (4-fluorophenyl)trimethyl-, CID136298, 455-17-4
• IUPAC Name: (4-fluorophenyl)-trimethylsilane
• SMILES: C[Si](C)(C)C1=CC=C(C=C1)F
• InChI Key: VZKFVPRKXHZBQO-UHFFFAOYSA-N
• Boiling Point: 175.6ºC at 760mmHg
• Flash Point: 60ºC
• Density: 0.93g/cm³
• Appearance: Transparent liquid
• Exact Mass: 168.07700
• H-Bond Acceptor: 1
• H-Bond Donor: 0
• Packaging: 10 g; 100 g
• Safety Description: 16

Custom Q&A

What is the molecular formula of 4-Fluorophenyltrimethylsilane?

The molecular formula of 4-Fluorophenyltrimethylsilane is C9H13FSi.

What is the molecular weight of 4-Fluorophenyltrimethylsilane?

The molecular weight of 4-Fluorophenyltrimethylsilane is 168.28 g/mol.

What is the IUPAC name of 4-Fluorophenyltrimethylsilane?

The IUPAC name of 4-Fluorophenyltrimethylsilane is (4-fluorophenyl)-trimethylsilane.

What is the InChI of 4-Fluorophenyltrimethylsilane?

The InChI of 4-Fluorophenyltrimethylsilane is InChI=1S/C9H13FSi/c1-11(2,3)9-6-4-8(10)5-7-9/h4-7H,1-3H3.

What is the InChIKey of 4-Fluorophenyltrimethylsilane?

The InChIKey of 4-Fluorophenyltrimethylsilane is VZKFVPRKXHZBQO-UHFFFAOYSA-N.

What is the CAS number of 4-Fluorophenyltrimethylsilane?

The CAS number of 4-Fluorophenyltrimethylsilane is 455-17-4.

How many hydrogen bond donor counts does 4-Fluorophenyltrimethylsilane have?

4-Fluorophenyltrimethylsilane has 0 hydrogen bond donor counts.

How many hydrogen bond acceptor counts does 4-Fluorophenyltrimethylsilane have?

4-Fluorophenyltrimethylsilane has 1 hydrogen bond acceptor count.

How many rotatable bond counts does 4-Fluorophenyltrimethylsilane have?

4-Fluorophenyltrimethylsilane has 1 rotatable bond count.

What is the formal charge of 4-Fluorophenyltrimethylsilane?

The formal charge of 4-Fluorophenyltrimethylsilane is 0.

Synthetic Use

Upstream Synthesis Route 1

• 462-06-6
• 1450-14-2

• 13183-70-5
• 455-17-4
• 1842-26-8
• 17151-09-6

Reference: [1] Organic letters, 2001, vol. 3, # 8, p. 1197 - 1200

Upstream Synthesis Route 2

• 75-77-4
• 352-13-6

• 455-17-4

Reference: [1]Roberts, J. D.; McElhill, E. A.; Armstrong, R.
[Journal of the American Chemical Society, 1949, vol. 71, p. 2923 - 2926]
[2][Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Si: MVol.C, 22, page 68 - 71]
[3]Roberts; McElhill; Armstrong
[Journal of the American Chemical Society, 1949, vol. 71, p. 2923,2926]
[4]Pearson, Anthony J.; Gontcharov, Alexander V.
[Journal of Organic Chemistry, 1998, vol. 63, # 1, p. 152 - 162]
[5]Funaki, Kenji; Kawai, Hiroshi; Sato, Tetsuo; Oi, Shuichi
[Chemistry Letters, 2011, vol. 40, # 9, p. 1050 - 1052]

Upstream Synthesis Route 3

• 75-77-4
• 460-00-4

• 455-17-4

Reference: [1]Harper, Matthew J.; Emmett, Edward J.; Bower, John F.; Russell, Christopher A.
[Journal of the American Chemical Society, 2017, vol. 139, # 36, p. 12386 - 12389]

Downstream Synthesis Route 1

• 1003-09-4
• 455-17-4

• 4805-22-5
• 1073313-97-9
• 398-23-2

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

Downstream Synthesis Route 2

• 455-17-4

• 70-34-8
• 350-46-9

Reference: [1] Journal of Fluorine Chemistry, 1998, vol. 92, # 1, p. 27 - 32

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