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Phenylphosphonic dichloride

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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
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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.)
Flash point:
>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 Gravity
1.394 (25℃)
Water Solubility 
reacts
Sensitive 
Moisture Sensitive
λmax
267nm(Cyclohexane)(lit.)
BRN 
1072240
Dielectric constant
26.0
InChIKey
IBDMRHDXAQZJAP-UHFFFAOYSA-N
LogP
1.089 at 20℃
CAS DataBase Reference
824-72-6(CAS DataBase Reference)
NIST Chemistry Reference
Phosphonic dichloride, phenyl-(824-72-6)
EPA Substance Registry System
Phosphonic dichloride, P-phenyl- (824-72-6)
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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
Toxicity
LD50 orally in Rabbit: 681 mg/kg

MSDS

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Phenylphosphonic dichloride Usage And Synthesis

Chemical Properties

Colorless to light yellow liqui

Uses

Phenylphosphonic 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 Methods

Fractionally 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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