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Dichlorophenylphosphine, 97%, Thermo Scientific Chemicals
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Catalog number A10284.18
also known as A10284-18
Price (USD)/ Each
32.10
-
Quantity:
50 g
Price (USD)/ Each
32.10
Dichlorophenylphosphine, 97%, Thermo Scientific Chemicals
Catalog numberA10284.18
Price (USD)/ Each
32.10
-
Chemical Identifiers
CAS644-97-3
IUPAC Namedichloro(phenyl)phosphane
Molecular FormulaC6H5Cl2P
InChI KeyIMDXZWRLUZPMDH-UHFFFAOYSA-N
SMILESClP(Cl)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
Assay (GC)≥96.0%
Identification (FTIR)Conforms
FormLiquid
Refractive Index1.5950-1.6000 @ 20?C
Dichlorophenylphosphine and its derivatives are used as an intermediate to make plasticizers, antioxidants, stabilizers, catalysts and high pressure lubricant additives and in lacquer formulatings.
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
Dichlorophenylphosphine and its derivatives are used as an intermediate to make plasticizers, antioxidants, stabilizers, catalysts and high pressure lubricant additives and in lacquer formulatings.
Solubility
Reacts with water.
Notes
Air & moisture Sensitive. Incompatible with bases, oxidizing agents, water/ moisture & air. Store under inert gas.
Dichlorophenylphosphine and its derivatives are used as an intermediate to make plasticizers, antioxidants, stabilizers, catalysts and high pressure lubricant additives and in lacquer formulatings.
Solubility
Reacts with water.
Notes
Air & moisture Sensitive. Incompatible with bases, oxidizing agents, water/ moisture & air. Store under inert gas.
RUO – Research Use Only
General References:
- Vladimir P. Novikov; Svein Samdal; Lev V. Vilkova. Determination of the molecular structure and the internal rotation potential of dichlorophenylphosphine using gas electron diffraction and relaxation constraints from ab initio calculations. Journal of molecular structure.1997, 413-414 279-292.
- Reacts with chlorine to give phenylphosphorus tetrachloride, which, with unactivated phenols at moderately elevated temperatures, gives aryl chlorides: J. Org. Chem., 55, 3415 (1990).