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Thermo Scientific Chemicals
Diphenyldichlorosilane, 97%
CAS: 80-10-4 | C12H10Cl2Si | 253.20 g/mol
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Catalog number A12051.36
also known as A12051-36
Price (USD)
151.65
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168.00Save 16.35 (10%)
Each
Quantity:
500 g
Price (USD)
151.65
Online Exclusive
168.00Save 16.35 (10%)
Each
Chemical Identifiers
CAS80-10-4
IUPAC Namedichlorodiphenylsilane
Molecular FormulaC12H10Cl2Si
InChI KeyOSXYHAQZDCICNX-UHFFFAOYSA-N
SMILESCl[Si](Cl)(C1=CC=CC=C1)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetIdentification (FTIR)Conforms
Assay (unspecified)≥96.0%
FormLiquid
Refractive Index1.5785-1.5835 @ 20?C
Appearance (Color)Clear colorless to pale yellow
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dye stuffs.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dye stuffs.
Solubility
Decomposes in water.
Notes
Moisture Sensitive. Store away from water/moisture, oxidizing agents and bases. Store under inert gas.
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dye stuffs.
Solubility
Decomposes in water.
Notes
Moisture Sensitive. Store away from water/moisture, oxidizing agents and bases. Store under inert gas.
RUO – Research Use Only
General References:
- P Huttenloch.; K E Roehl.; K Czurda. Sorption of nonpolar aromatic contaminants by chlorosilane surface modified natural minerals.Environ Sci Technol.2001,35(21), 4260-4264.
- R V Lewis.; A Fallon.; S Stein.; K D Gibson.; S Udenfriend. Supports for reverse-phase high-performance liquid chromatography of large proteins.Anal Biochem.1980,104(1), 153-159.
- Silylating agent (see Appendix 4) for formation of diphenylsilylene derivatives of diols. Silylation occurs faster in the presence of pyridine bases than with triethylamine and is accelerated by the addition of DMAP: J. Organomet. Chem., 271, 327 (1984); Canad. J. Chem., 64, 1450 (1986). The group is readily cleaved by hydrolysis or with F-.