Chloromethyldimethylisopropoxysilane

• CAS: 18171-11-4
• Catalog Number: ACM18171114
• Category: Siloxanes
• Molecular Weight: 166.73 g/mol
• Molecular Formula: C6H15ClOSi
• Synonyms: (Chloromethyl)dimethylisopropoxysilane; CHLOROMETHYLDIMETHYLISOPROPOXYSILANE; (ChloroMethyl)isopropoxydiMethylsilane; (Chloromethyl)(isopropoxy)dimethylsilane
• IUPAC Name: chloromethyl-dimethyl-propan-2-yloxysilane
• Canonical SMILES: CC(C)O[Si](C)(C)CCl
• InChI Key: KOTFCAKXPLOYLN-UHFFFAOYSA-N
• Boiling Point: 142 °C(760 mmHg)
• Flash Point: 28.3 °C
• Density: 0.918 g/mL
• Appearance: Transparent liquid
• Exact Mass: 166.05800
• Hazard Statements: Xi: Irritant
• Packaging: 10 g; 100 g
• Packing Group: III
• Safety Description: S26
• WGK Germany: 3

Custom Q&A

What is the molecular formula of Chloromethyldimethylisopropoxysilane?

The molecular formula is C6H15ClOSi.

What is the molecular weight of Chloromethyldimethylisopropoxysilane?

The molecular weight is 166.72 g/mol.

What is the IUPAC name of Chloromethyldimethylisopropoxysilane?

The IUPAC name is chloromethyl-dimethyl-propan-2-yloxysilane.

What is the InChI of Chloromethyldimethylisopropoxysilane?

The InChI is InChI=1S/C6H15ClOSi/c1-6(2)8-9(3,4)5-7/h6H,5H2,1-4H3.

What is the InChIKey of Chloromethyldimethylisopropoxysilane?

The InChIKey is KOTFCAKXPLOYLN-UHFFFAOYSA-N.

What is the canonical SMILES of Chloromethyldimethylisopropoxysilane?

The canonical SMILES is CC(C)O[Si](C)(C)CCl.

What is the CAS number of Chloromethyldimethylisopropoxysilane?

The CAS number is 18171-11-4.

What is the EC number of Chloromethyldimethylisopropoxysilane?

The EC number is 628-137-7.

What is the DSSTox Substance ID of Chloromethyldimethylisopropoxysilane?

The DSSTox Substance ID is DTXSID10295607.

Is Chloromethyldimethylisopropoxysilane a covalently-bonded unit?

Yes, Chloromethyldimethylisopropoxysilane is a covalently-bonded unit.

Synthetic Use

Upstream Synthesis Route 1

• 1719-57-9
• 67-63-0

• 18171-11-4

Reference: [1]Tamao, Kohei; Ishida, Neyoshi; Ito, Yoshihiko; Kumada, Makoto
[Organic Syntheses, 1990, vol. 69, p. 96 - 96]
[2]Ehbets, Julia; Lorenzen, Sabine; Mahler, Christoph; Bertermann, Rüdiger; Berkefeld, André; Poater, Jordi; Fritz-Langhals, Elke; Weidner, Richard; Bickelhaupt, F. Matthias; Tacke, Reinhold
[European Journal of Inorganic Chemistry, 2016, vol. 2016, # 11, p. 1641 - 1659]
[3]Andrianov,K.A. et al.
[Journal of general chemistry of the USSR, 1975, vol. 45, p. 2614 - 2618][Zhurnal Obshchei Khimii, 1975, vol. 45, # 12, p. 1652 - 1657]
Andrianow; Golubenko
[Doklady Akademii Nauk SSSR, 1957, vol. 112, p. 257][Doklady Chemistry, 112-117<1957>25]

Downstream Synthesis Route 1

• 18171-11-4
• 127-08-2

• 58307-35-0

Reference: [1]Andrianov,K.A. et al.
[Journal of general chemistry of the USSR, 1975, vol. 45, p. 2614 - 2618][Zhurnal Obshchei Khimii, 1975, vol. 45, # 12, p. 1652 - 1657]

Downstream Synthesis Route 2

• 40653-15-4
• 18171-11-4

• 127588-70-9

Reference: [1]Garegg, Per J.; Oscarson, Stefan; Szoenyi, Maria
[Carbohydrate Research, 1990, vol. 205, # 1, p. 125 - 132]

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