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Diphenyl Phosphite

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Name

Diphenyl Phosphite

EINECS 225-202-8
CAS No. 4712-55-4 Density 1.223 g/mL at 25 °C(lit.)
PSA 59.00000 LogP 3.53410
Solubility N/A Melting Point 12 °C(lit.)
Formula C12H11O3P Boiling Point 348.233 °C at 760 mmHg
Molecular Weight 234.191 Flash Point 178.834 °C
Transport Information N/A Appearance clear liquid
Safety 26-39 Risk Codes 22-37/38-41
Molecular Structure Molecular Structure of 4712-55-4 (Diphenyl Phosphite) Hazard Symbols HarmfulXn
Synonyms

Diphenoxyphosphine oxide;Diphenyl hydrogenphosphite;Doverphos 213;NSC43786;

Article Data 29

Diphenyl Phosphite Synthetic route

101-02-0

triphenyl phosphite

4712-55-4

diphenyl hydrogen phosphite

Conditions
ConditionsYield
With trifluorormethanesulfonic acid; water at 25℃; Sealed tube;91%
With phosphonic acid
With water
108-95-2

phenol

4712-55-4

diphenyl hydrogen phosphite

Conditions
ConditionsYield
With trichlorophosphate In toluene at 70℃; for 1.8h; Temperature;71.3%
With tetraethylammonium iodide; water In acetonitrile at 50℃; electrosynthesis;20%
With tetraethyldiamidophosphite
With phosphorus trichloride
With trichlorophosphate In toluene at 50℃; for 1.7h;
108-95-2

phenol

A

2310-89-6

phenyl hydrogen phosphonate

B

4712-55-4

diphenyl hydrogen phosphite

Conditions
ConditionsYield
With hypophosphorous acid In toluene for 72h; Reflux; Dean-Stark; Inert atmosphere;A n/a
B 63%
With P4O6 In benzene for 1h; Title compound not separated from byproducts;
With P4O6 In benzene for 1h;
5382-00-3

Diphenyl phosphorochloridite

4712-55-4

diphenyl hydrogen phosphite

Conditions
ConditionsYield
With pyridine; diethyl ether; water
Multi-step reaction with 2 steps
1: pyridine
2: hydrogen chloride / 0 °C
View Scheme
14862-35-2

phosphoric acid diphenyl ester-propyl ester

4712-55-4

diphenyl hydrogen phosphite

Conditions
ConditionsYield
With hydrogenchloride at 0℃;
101-02-0

triphenyl phosphite

598-02-7

Diethyl phosphate

A

2510-86-3

O,O-diethyl O-phenyl phosphate

B

4712-55-4

diphenyl hydrogen phosphite

Conditions
ConditionsYield
In nitromethane at 30℃;
101-02-0

triphenyl phosphite

598-02-7

Diethyl phosphate

A

4712-55-4

diphenyl hydrogen phosphite

B

(Phosphorigsaeure-diphenylester)-(Phosphorsaeure-diethylester)anhydrid

Conditions
ConditionsYield
In nitromethane at 30℃; for 8h; Mechanism; Heating; other reactants, other products, other solvents, other temperatures;
101-02-0

triphenyl phosphite

A

4712-55-4

diphenyl hydrogen phosphite

B

108-95-2

phenol

Conditions
ConditionsYield
With hydrogenchloride In ethanol at 25℃; Rate constant; effect of micelles (sodium lauryl sulfate, dodecylhydrogensulfuric acid, n-tetradecansulfonic acid, p-decyloxybenzenesulfonic acid, cetyltrimethylammonium chloride) and electrolytes;
108-95-2

phenol

A

4712-55-4

diphenyl hydrogen phosphite

B

54921-72-1

phenyl H-phosphonate ammonium salt

Conditions
ConditionsYield
With P4O6; ammonia 1.) benzene, 1 h; 2.) benzene; Multistep reaction;
180906-75-6

C11H15O4P

108-95-2

phenol

4712-55-4

diphenyl hydrogen phosphite

Diphenyl Phosphite Specification

This chemical is called Phosphonic acid, diphenyl ester, and it can also be named as Diphenyl phosphonate. With the molecular formula of C12H11O3P, its molecular weight is 234.19. The CAS registry number of this chemical is 4712-55-4. Additionally, its product categories are Organic Building Blocks; Organic Phosphates/Phosphites; Phosphorus Compounds.

Other characteristics of the Phosphonic acid, diphenyl ester can be summarised as followings: (1)ACD/LogP: 0.91; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2; (4)ACD/LogD (pH 7.4): 2; (5)ACD/BCF (pH 5.5): 28; (6)ACD/BCF (pH 7.4): 28; (7)ACD/KOC (pH 5.5): 373; (8)ACD/KOC (pH 7.4): 373; (9)#H bond acceptors: 3; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 4; (12)Polar Surface Area: 59 Å2; (13)Flash Point: 178.834 °C; (14)Enthalpy of Vaporization: 56.918 kJ/mol; (15)Boiling Point: 348.233 °C at 760 mmHg; (16)Vapour Pressure: 0 mmHg at 25°C.

Production method of this chemical: The Phosphonic acid, diphenyl ester could be obtained by the reactant of phenol. This reaction needs the reagent of (Et2N)2P(O)H.

Uses of this chemical: The phenyl H-phosphonate ammonium salt could be obtained by the reactant of Phosphonic acid, diphenyl ester. This reaction needs the reagent of pyridine, aq. NH3, and the solvent of H2O. The yield is 89 %.

When you are using this chemical, please be cautious about it as the following: This chemical is irritating to respiratory system and skin. It's harmful if swallowed. It has risk of serious damage to the eyes.Wear eye / face protection if you use it. In case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
1.InChI:InChI=1/C12H11O3P/c13-16(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10,16H
2.Smiles: P(Oc1ccccc1)(=O)Oc1ccccc1

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