Phenylphosphonic dichloride

Phenylphosphonic dichloride
  • CAS No.:824-72-6
Other grades of this product :
Phenylphosphonic dichloride Basic information
Product Name:Phenylphosphonic dichloride
Synonyms:Benzenephosphonicaciddichloride;Benzenephosphonyl chloride;BPOD;AURORA KA-1395;BENZENEPHOSPHONIC DICHLORIDE;Benzene phosphorus oxychloride;BENZENE PHOSPHORUS OXYDICHLORIDE;phenyl-phosphonicdichlorid
CAS:824-72-6
MF:C6H5Cl2OP
MW:194.98
EINECS:212-534-3
Product Categories:organophosphorus compound;Ligand
Mol File:824-72-6.mol
Phenylphosphonic dichloride Chemical Properties
Melting point 3 °C(lit.)
Boiling point 258 °C(lit.)
density 1.375 g/mL at 25 °C(lit.)
vapor pressure 2.36Pa at 25℃
refractive index n20/D 1.559(lit.)
Fp >230 °F
storage temp. Store below +30°C.
solubility Miscible with benzene, chloroform, dimethyl sulfoxide and carbon tetrachloride.
form Liquid
color Clear yellow to brown
Specific Gravity1.394 (25℃)
Water Solubility reacts
Sensitive Moisture Sensitive
λmax267nm(Cyclohexane)(lit.)
BRN 1072240
InChIKeyIBDMRHDXAQZJAP-UHFFFAOYSA-N
LogP1.089 at 20℃
CAS DataBase Reference824-72-6(CAS DataBase Reference)
NIST Chemistry ReferencePhosphonic dichloride, phenyl-(824-72-6)
EPA Substance Registry SystemPhosphonic dichloride, P-phenyl- (824-72-6)
Safety Information
Hazard Codes C
Risk Statements 14-34-37
Safety Statements 26-45-8-36/37/39
RIDADR UN 3265 8/PG 2
WGK Germany 3
TSCA Yes
HazardClass 8
PackingGroup II
HS Code 29310095
ToxicityLD50 orally in Rabbit: 681 mg/kg
MSDS Information
ProviderLanguage
Benzene phosphorous oxydichloride English
SigmaAldrich English
ACROS English
ALFA English
Phenylphosphonic dichloride Usage And Synthesis
Chemical PropertiesColorless to light yellow liqui
UsesPhenylphosphonic dichloride is used in the preparation of 2-phenyl-[1,3,2]dioxaphosphepane-2-oxide. Further, it acts as an effective reagent for the chlorinative dehydration of some heterocycles.
Synthesis Reference(s)Tetrahedron Letters, 33, p. 7473, 1992 DOI: 10.1016/S0040-4039(00)60798-0
Purification MethodsFractionally distil it using a very efficient or a spinning band column. [Lecher et al. J Am Chem Soc 76 1045 1954, NMR: Müller et al. J Am Chem Soc 78 3557 1956, Van Wazer et al. J Am Chem Soc 78 5715 1956, IR: Daasch & Smith Anal Chem 23 853 1951, Beilstein 16 IV 1074.]

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