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Phenylphosphonic dichloride

technical grade, 90%

Sinónimos:

Benzenephosphonic dichloride, Benzenephosphonyl chloride, Phenyldichlorophosphine oxide, Phenylphosphonyl dichloride, Phenylphosphoryl dichloride, P,P-Dichlorophenylphosphine oxide

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About This Item

Fórmula lineal:
C6H5POCl2
Número de CAS:
824-72-6
Peso molecular:
194.98
Beilstein/REAXYS Number:
1072240
EC Number:
212-534-3
MDL number:
MFCD00002070
UNSPSC Code:
12352106
PubChem Substance ID:
24864291
NACRES:
NA.22

grade

technical grade

assay

90%

form

liquid

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand

refractive index

n20/D 1.559 (lit.)

bp

258 °C (lit.)

mp

3 °C (lit.)

density

1.375 g/mL at 25 °C (lit.)

SMILES string

ClP(Cl)(=O)c1ccccc1

InChI

1S/C6H5Cl2OP/c7-10(8,9)6-4-2-1-3-5-6/h1-5H

InChI key

IBDMRHDXAQZJAP-UHFFFAOYSA-N

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Application

Phenylphosphonic dichloride (PPDC) is an organophosphorus compound with flame-retardant properties.
It can be used:
  • In the synthesis of PBPP (3,9-diphenyl-3,9-dioxa-2,4,8,10-tetraoxa-3,9-diphosphaspiro-5,5-undecane), another organo-phosphorus flame retardant.
  • As a reactant in the synthesis of perfluoroalkyl(phenyl)phosphinic acids from perfluoroalkyl Grignard reagents.
  • As a starting material for the synthesis of benzoxazine monomer containing phenylphosphine oxide which can be polymerized via ring-opening polymerization.
  • As a chlorinating agent for the conversion of thienopyrimidinedione into 4,6-dichlorothienopyrimidine.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

supp_hazards

EUH014

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

399.2 °F

flash_point_c

204 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Thermal degradation properties of wood reacted with diethylchlorophosphate or phenylphosphonic dichloride as potential flame retardants
Ellis WD, et al.
Wood and Fiber Science, 19(4), 439-445 (2007)
A study of the reaction of perfluoroalkyl Grignard reagents with phosphoryl chloride and phenylphosphonic dichloride
Hosein AI and Caffyn AJM
Dalton Transactions, 41(43), 13504-13508 (2012)
Thienopyrimidine-based P2Y12 platelet aggregation inhibitors
Kortum SW, et al.
Bioorganic & medicinal chemistry letters, 19(20), 5919-5923 (2009)
Synthesis and applications of biscyclic phosphorus flame retardants
Hoang D and Kim J
Polymer Degradation and Stability, 93(1), 36-42 (2008)
Synthesis, characterization and thermal degradation of functional benzoxazine monomers and polymers containing phenylphosphine oxide.
Choi S-W, et al.
Polymer Degradation and Stability, 91(5), 1166-1178 (2006)

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