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Thermo Scientific Chemicals
Dichlorophenylphosphine, 97%
CAS: 644-97-3 | C6H5Cl2P | 178.98 g/mol
化学物質識別子
CAS644-97-3
IUPAC Namedichloro(phenyl)phosphane
Molecular FormulaC6H5Cl2P
InChI KeyIMDXZWRLUZPMDH-UHFFFAOYSA-N
SMILESClP(Cl)C1=CC=CC=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless to pale yellow
Assay (GC)≥96.0%
Identification (FTIR)Conforms
Refractive Index1.5950-1.6000 @ 20?C
FormLiquid
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).