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P22389

Sigma-Aldrich

Phenyl dichlorophosphate

≥95%

Sinonimo/i:

Phenyl phosphodichloridate, Phenyl phosphorodichloridate, Phenyl phosphoryl dichloride

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About This Item

Formula condensata:
C6H5OP(O)Cl2
Numero CAS:
770-12-7
Peso molecolare:
210.98
Beilstein:
511863
Numero CE:
212-220-6
Numero MDL:
MFCD00002067
Codice UNSPSC:
12352100
ID PubChem:
24898297
NACRES:
NA.22

Livello qualitativo

200

Saggio

≥95%

Indice di rifrazione

n20/D 1.523 (lit.)

P. eboll.

241-243 °C (lit.)

Densità

1.412 g/mL at 25 °C (lit.)

Stringa SMILE

ClP(Cl)(=O)Oc1ccccc1

InChI

1S/C6H5Cl2O2P/c7-11(8,9)10-6-4-2-1-3-5-6/h1-5H
TXFOLHZMICYNRM-UHFFFAOYSA-N

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Applicazioni

Reagent for the preparation of phosphate diesters.

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H314

Classi di pericolo

Skin Corr. 1B

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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The Journal of Organic Chemistry, 53, 2077-2077 (1988)
Chun-Wei Kuo et al.
Molecules (Basel, Switzerland), 17(11), 13662-13672 (2012-11-22)
Upon treatment with phenyl dichlorophosphate (PhOP=OCl(2)) in acetonitrile at ambient temperature, a variety of ketoximes underwent a Beckmann rearrangement in an effective manner to afford the corresponding amides in moderate to high yields.
Xiaoming Zhou et al.
Chemosphere, 235, 163-168 (2019-07-01)
Two novel phosphorus-containing copolyesters were synthesized by direct polycondensation reaction of phenyl dichlorophosphate, 1,4-succinic acid and 1,4-butanediol using stannous chloride (SnCl2) and 4-Methylbenzenesulfonic acid as catalyst, and its chemical structures were identified by 1H and 31P nuclear magnetic resonances (1H
Yvan Ecochard et al.
Molecules (Basel, Switzerland), 24(9) (2019-05-15)
Epoxy materials have attracted attention for many applications that require fireproof performance; however, the utilization of hazardous reagents brings about potential damage to human health. Eugenol and cardanol are renewable, harmless resources (according to ECHA) that allow the achievement of
R M Dawson et al.
Analytical biochemistry, 170(2), 451-455 (1988-05-01)
An improved method for assaying carbamylated acetylcholinesterase is described which has substantial benefits over current methods. Acetylcholinesterase was carbamylated with neostigmine and diluted extensively into buffer to allow decarbamylation to occur. At various times, phenyldichlorophosphate was added to the mixture
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