diethyl pyren-1-ylmethyl phosphate
Diethyl phosphate
Conditions | Yield |
---|---|
In methanol; benzene for 2h; Product distribution; Quantum yield; Irradiation; other phosphates; var. solvents; | 100% |
benzaldehyde
A
Diethyl phosphate
B
α-methyltrans-cinnamyl N-phenylimine
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 25℃; for 3h; | A n/a B 98% |
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran for 0.5h; | 95% |
With sodium hydroxide In tetrahydrofuran; water at 0℃; | 92% |
With sodium hydroxide at 30 - 40℃; | 90% |
tetrachlorobis[4-(dimethylamino)pyridine]phosphorus(V) chloride
ethanol
Diethyl phosphate
Conditions | Yield |
---|---|
at 60℃; for 4.5h; | 95% |
cis-tetrachlorobis(1-methylimidazole)phosphorus(V) chloride
ethanol
Diethyl phosphate
Conditions | Yield |
---|---|
at 60℃; for 4.5h; | 95% |
Diethyl 2-(methylsulfonylamino)phenyl phosphate
A
Diethyl phosphate
B
N-cyclohexylmethanesulfonamide
Conditions | Yield |
---|---|
With hydrogen; acetic acid; trifluoroacetic acid; platinum(IV) oxide at 20℃; under 750.06 Torr; for 20h; | A 93% B 73% |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In benzene at 80℃; for 4h; Inert atmosphere; | 93% |
With trifluorormethanesulfonic acid In toluene at 120℃; for 24h; Sealed tube; Schlenk technique; Inert atmosphere; | 93% |
(diethoxy phosphoryl) fluoroacetic acid
benzaldehyde
A
Diethyl phosphate
B
(Z)-2-fluoro-3-phenylacrylic acid
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; hexane 1.) -78 deg C, 1 h; 2.) 15 h room temperature; | A n/a B 91% |
(diethoxy phosphoryl) fluoroacetic acid
4-methoxy-benzaldehyde
A
Diethyl phosphate
B
(Z)-2-fluoro-3-(4-methoxyphenyl)-2-propenoic acid
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; hexane 1.) -78 deg C, 1 h; 2.) 15 h room temperature; | A n/a B 90% |
phosphonic acid diethyl ester
A
Diethyl phosphate
B
Tetraethyl pyrophosphate
Conditions | Yield |
---|---|
With iodosylbenzene In tetrahydrofuran for 48h; Heating; | A 90% B 5% |
With iodosylbenzene In benzene for 0.5h; Product distribution; Further Variations:; Solvents; Heating; | A 11% B 77% |
With iodosylbenzene In benzene for 0.5h; Heating; | A 11% B 77% |
Conditions | Yield |
---|---|
With oxygen; hypophosphorous acid; copper dichloride at 70℃; for 6h; | A 89% B 4% |
ethanol
phosphonic acid diethyl ester
A
Diethyl phosphate
B
triethyl phosphate
Conditions | Yield |
---|---|
With tetraethylammonium iodide; water In acetonitrile at 25℃; Product distribution; var. ethanol:H2O ratios; electrosynthesis; | A 12.5% B 86.1% |
Conditions | Yield |
---|---|
With tetraethylammonium iodide; water In ethanol; acetonitrile at 25℃; | A 12.5% B 86.1% |
N,N'-di-(2,2,6,6-tetramethyl-1-oxyl-piperidin-4-yl)-N-diethylphosphorylurea
A
Diethyl phosphate
B
di-(2,2,6,6-tetramethyl-1-oxyl-piperidin-4-yl)carbodiimide
Conditions | Yield |
---|---|
With sodium hydride In 1,2-dimethoxyethane 1. ) 20 deg C, 6 h, 2.) reflux, 2 h; | A n/a B 86% |
diethyl (2-(4-methoxyphenyl)-2-oxoethyl) phosphate
A
Diethyl phosphate
B
1-(4-methoxyphenyl)ethanone
Conditions | Yield |
---|---|
With 1,4-dioxane; triethylamine at -20℃; for 8h; Mechanism; Product distribution; Irradiation; | A 86% B 84% |
Phosphoric acid 2-chloro-6-methanesulfonylamino-phenyl ester diethyl ester
A
Diethyl phosphate
Conditions | Yield |
---|---|
With hydrogen; platinum(IV) oxide In acetic acid; trifluoroacetic acid at 20℃; under 750.06 Torr; for 20h; | A 85% B 70% |
Phosphoric acid 2,4-dichloro-6-methanesulfonylamino-phenyl ester diethyl ester
A
Diethyl phosphate
Conditions | Yield |
---|---|
With hydrogen; platinum(IV) oxide In acetic acid; trifluoroacetic acid at 20℃; under 750.06 Torr; for 20h; | A 85% B 70% |
ethanol
A
ethyl phosphate
B
Diethyl phosphate
C
triethyl phosphate
Conditions | Yield |
---|---|
With phosphorus; tetraethylammonium iodide In water; acetonitrile electrolysis; | A n/a B n/a C 84% |
Conditions | Yield |
---|---|
With HKUST-1 metal organic framework In chloroform at 20℃; Kinetics; | 83% |
Conditions | Yield |
---|---|
With di-iodine pentaoxide In acetonitrile at 80℃; for 12h; | 82% |
With oxygen; silver nitrate In toluene at 60℃; for 1h; | 37% |
With iodosylbenzene In acetonitrile at 20℃; for 180h; | 29% |
With iodide; iodine; carbonate(2-) at 25℃; Rate constant; various catalysts, reagent and catalyst concentration, isotope effect; |
bromo-1 hydroxy-2 ethyl phosphonate de diethyle
A
epoxy-1,2 ethyl phosphonate de diethyle
B
Diethyl phosphate
C
α-bromovinylphosphonic acid diethyl ester
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran for 2h; Ambient temperature; | A 82% B 5% C n/a |
O,O,O-triethyl phosphorothioate
A
Diethyl phosphate
B
ethylphosphonic acid diethyl ester
C
phosphonic acid diethyl ester
Conditions | Yield |
---|---|
With magnesium monoperoxyphthalate hexahydrate In water at 25℃; for 24h; | A 10% B 81% C 9% |
[2-(4,5-Dimethyl-2-piperidin-1-yl-[1,3]dithiol-2-yl)-benzo[1,3]dithiol-2-yl]-phosphonic acid diethyl ester
A
1-piperidin-1-yl-ethanone
B
dimethyl benzotetrathiafulvalene
C
Diethyl phosphate
D
piperdinium acetate
Conditions | Yield |
---|---|
With acetic acid Ambient temperature; AcOH : Educt ratio = 10; | A n/a B 80% C n/a D n/a |
With acetic acid Ambient temperature; AcOH : Educt ratio = 10; Yield given; |
Conditions | Yield |
---|---|
With HKUST-1 metal organic framework In chloroform at 20℃; Kinetics; | 78% |
With 7,7'-carbonylbis(azanediyl)bis(N-butyl-1H-indole-2-carboxamide) In water; acetone at 25℃; | |
With K12(Ti2O2)(GeNb12O40)*19H2O; water In N,N-dimethyl-formamide at 20℃; for 0.5h; Reagent/catalyst; |
Conditions | Yield |
---|---|
With hydrogenchloride In acetone -5 deg C, 1 h then 20 deg C, 2 h; | A n/a B 77% |
Conditions | Yield |
---|---|
Product distribution; multistep reaction, var. aldehydes.; | A n/a B 71% |
With hydrogenchloride 1.) THF, 0 to 20 deg C, 3 h, 2.) ether; Yield given. Multistep reaction; |
Thiophosphorsaeure-O,O-diethylester
A
Diethyl phosphate
B
phosphonic acid diethyl ester
Conditions | Yield |
---|---|
With magnesium monoperoxyphthalate hexahydrate In water at 25℃; for 24h; | A 70% B 30% |
O,O-diethyl phthalimido-phosphonothioate
A
Diethyl phosphate
B
phosphonic acid diethyl ester
Conditions | Yield |
---|---|
With magnesium monoperoxyphthalate hexahydrate In water at 25℃; for 24h; | A 27% B 70% |
Conditions | Yield |
---|---|
Product distribution; multistep reaction, var. aldehydes.; | A n/a B 66% |
With hydrogenchloride 1.) THF, 0 to 25 deg C, 3 h, 2.) ether; Yield given. Multistep reaction; |
benzaldehyde
diethyl (α-thiocyanatomethyl)phosphonate
A
Diethyl phosphate
B
(E)-(2-thiocyanatovinyl)-benzene
C
(Z)-diethyl styrylphosphonate
D
diethyl (E)-(2-phenylethenyl)phosphonate
Conditions | Yield |
---|---|
With potassium tert-butylate In tetrahydrofuran at -70℃; for 2h; | A n/a B n/a C 60% D n/a |
Diethyl phosphate
Conditions | Yield |
---|---|
With potassium tert-butylate In N,N-dimethyl-formamide at 20℃; for 0.25h; | 98% |
Diethyl phosphate
Conditions | Yield |
---|---|
at 80℃; for 5h; | 96.3% |
Diethyl phosphate
prinaberel
diethyl 2-fluoro-4-(5-hydroxy-7-vinylbenzo[d]oxazol-2-yl)phenyl phosphate
Conditions | Yield |
---|---|
With dmap; N-ethyl-N,N-diisopropylamine In tetrahydrofuran; tetrachloromethane; acetonitrile at 20℃; for 24h; | 93% |
Conditions | Yield |
---|---|
With magnesium(II) perchlorate In acetonitrile at 70 - 80℃; Kabachnik-Fields Reaction; | 93% |
Diethyl phosphate
tert-butyl 2-(6-(4-bromophenyl)pyridin-3-yl)propan-2-ylcarbamate
tert-butyl 2-(6-(4-(diethoxyphosphoryl)phenyl)pyridin-3-yl)propan-2-ylcarbamate
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; triethylamine In toluene for 8h; Inert atmosphere; Reflux; | 92.4% |
hexamethyldisilathiane
Diethyl phosphate
diethyltrimethylsilyl phosphate
Conditions | Yield |
---|---|
at 50℃; for 0.5h; | 92% |
Diethyl phosphate
2-diazo-1-(4-hydroxy-3-methoxyphenyl)ethanone
diethyl (2-(4-hydroxy-3-methoxyphenyl)-2-oxoethyl) phosphate
Conditions | Yield |
---|---|
In benzene at 60℃; for 24h; | 92% |
Conditions | Yield |
---|---|
With magnesium(II) perchlorate In acetonitrile at 70 - 80℃; Kabachnik-Fields Reaction; | 92% |
Diethyl phosphate
Conditions | Yield |
---|---|
With stannic bromide | 91% |
Diethyl phosphate
benzoyl chloride
benzoic (diethyl phosphoric) anhydride
Conditions | Yield |
---|---|
With silver(l) oxide In acetonitrile at 20℃; for 5h; | 91% |
Conditions | Yield |
---|---|
With triethylamine; hexamethyltriaminodibromophosphorane In dichloromethane for 2h; Ambient temperature; | 91% |
Diethyl phosphate
2-diazomethyl-3-phenyl-4H-sulfonylchromen
(1,1-dioxido-4-oxo-3-phenyl-4H-thiochromen-2-yl)methyl diethyl phosphate
Conditions | Yield |
---|---|
With hydrogenchloride In chloroform; water at 60℃; for 3h; pH=4; Inert atmosphere; | 91% |
Diethyl phosphate
4-methoxy-benzaldehyde
diethyl [1-amine(4-methoxyphenyl)methyl]phosphonate
Conditions | Yield |
---|---|
With ammonium acetate at 20 - 60℃; for 44h; Molecular sieve; | 91% |
Conditions | Yield |
---|---|
With N,N,N',N'-tetramethylchlorformamidinium chloride; triethylamine In dichloromethane at 0 - 20℃; for 2h; | 90% |
Diethyl phosphate
(S)-S-ethyl 2-((tert-butoxycarbonyl)amino)propanethioate
Conditions | Yield |
---|---|
With potassium tert-butylate In toluene at 20℃; for 0.25h; | 90% |
Diethyl phosphate
Conditions | Yield |
---|---|
With potassium tert-butylate In toluene at 20℃; for 0.25h; | 90% |
N-(cyclobutylidene)-2-methyl-2-propanamine
Diethyl phosphate
Conditions | Yield |
---|---|
With titanium tetrachloride In neat liquid at 0℃; for 24h; | 90% |
Product Name: Diethyl phosphoric acid (CAS NO.598-02-7)
Molecular Formula: C4H11O4P
Molecular Weight: 154.1g/mol
Mol File: 598-02-7.mol
Einecs: 209-912-5
Appearance: Clear colorless to light yellow-orange liquid
Melting Point: 6 °C
Boiling point: 200.3 °C at 760 mmHg
Flash Point: 74.9 °C
Density: 1.195 g/cm3
Surface Tension: 37.6 dyne/cm
Enthalpy of Vaporization: 48.11 kJ/mol
Vapour Pressure: 0.137 mmHg at 25°C
XLogP3-AA: -0.3
H-Bond Donor: 1
H-Bond Acceptor: 4
Structure Descriptors of Diethyl phosphoric acid (CAS NO.598-02-7):
IUPAC Name: diethyl hydrogen phosphate
Canonical SMILES: CCOP(=O)(O)OCC
InChI: InChI=1S/C4H11O4P/c1-3-7-9(5,6)8-4-2/h3-4H2,1-2H3,(H,5,6)
InChIKey: UCQFCFPECQILOL-UHFFFAOYSA-N
Product Categories: Alphabetic; D; DID - DINEnvironmental Standards; Metabolites; Pesticides&Metabolites
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rat | LDLo | oral | > 250mg/kg (250mg/kg) | National Academy of Sciences, National Research Council, Chemical-Biological Coordination Center, Review. Vol. 5, Pg. 37, 1953. |
Reported in EPA TSCA Inventory.
A poison by ingestion. When heated to decomposition it emits toxic vapors of POx.
Safety Information of Diethyl phosphoric acid (CAS NO.598-02-7):
Hazard Codes: Xi
Risk Statements: 36/37/38
36: Irritating to the eyes
37: Irritating to the respiratory system
38: Irritating to the skin
Safety Statements: 37/39-26-36
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36: Wear suitable protective clothing
37: Wear suitable gloves
39: Wear eye/face protection
Diethyl phosphoric acid ,its CAS NO. is 598-02-7,the synonyms is Diethyl acid phosphate ; Diethyl hydrogen phosphate ; Diethyl phosphate ; EINECS 209-912-5 ; Ethyl phosphate, (ETO)2(HO)PO ; Ethyl phosphate, di- ; NSC 97178 ; O,O-Diethyl hydrogen phosphate ; Phosphoric acid, diethyl ester .
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View