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Details

Stereochemistry ACHIRAL
Molecular Formula C4H11O3P
Molecular Weight 138.1021
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Diethyl phosphite

SMILES

CCOP(=O)OCC

InChI

InChIKey=MJUJXFBTEFXVKU-UHFFFAOYSA-N
InChI=1S/C4H11O3P/c1-3-6-8(5)7-4-2/h8H,3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C4H11O3P
Molecular Weight 138.1021
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and characterization of diethoxy phosphoryl chitosan.
2010-11-01
Stereochemical effects in fragmentation of diastereoisomers of protected diethyl 1,2-diamino-alkylphosphonates.
2010-08-30
Intelligent chiral sensing based on supramolecular and interfacial concepts.
2010
Structure of EstA esterase from psychrotrophic Pseudoalteromonas sp. 643A covalently inhibited by monoethylphosphonate.
2009-09-01
Stereoselective synthesis of nipecotic acid derivatives via palladium-catalyzed decarboxylative cyclization of gamma-methylidene-delta-valerolactones with imines.
2009-01-15
rac-(1S,2R)-Diethyl 6-hydr-oxy-1-(4-methoxy-phen-yl)-3-oxo-2,3-di-hydro-1H-benzo[f]chromen-2-yl]-phospho-nate.
2008-06-07
Ethyl [(2-hydroxy-phen-yl)(pyridinium-2-ylamino)meth-yl]phospho-nate methanol solvate.
2008-06-07
Preparation of alpha-aminobenzylphosphonic acids with a stereogenic quaternary carbon atom via microscopically configurationally stable alpha-aminobenzyllithiums.
2008
Synthesis of lipophilic 2-oxoamides based on gamma-aminobutyric and delta-aminovaleric analogues and their activity against phospholipase A2.
2007-10
Temperature effects on stereocontrol in the Horner-Wadsworth-Emmons condensation of alpha-phosphono lactones.
2007-08-03
A new bisphosphonate-containing (99m)Tc(I) tricarbonyl complex potentially useful as bone-seeking agent: synthesis and biological evaluation.
2007-06
Diethyl [(Z)-1-iodo-2-phenyl-1-hexenyl]phosphonate.
2005-03
Influence of anionic functions on the coordination and photophysical properties of lanthanide(III) complexes with tridentate bipyridines.
2004-11-15
Synthesis and phosphodiesterase 5 inhibitory activity of new sildenafil analogues containing a phosphonate group in the 5(')-sulfonamide moiety of phenyl ring.
2004-05-03
Porphyrins bearing mono or tripodal benzylphosphonic acid tethers for attachment to oxide surfaces.
2004-03-05
New efficient procedure for the use of diethoxyphosphoryl as a protecting group in the synthesis of polyazamacrocycles. Preparation of polyazacyclophanes derived from resorcinol.
2003-12-26
Synthesis, crystal structure, and ESR study of a novel phosphorylated lipophilic spin trap.
2002-11-01
Effect of structural variation within lipophilic N-(X)sulfonyl carbamoyl lariat ethers on the selectivity and efficiency of competitive alkali metal cation extraction into chloroform.
2002-05-01
Phosphonate O-deethylation of [4-(4-bromo-2-cyano-phenylcarbamoyl) benzyl]-phosphonic acid diethyl ester, a lipoprotein lipase-promoting agent, catalyzed by cytochrome P450 2C8 and 3A4 in human liver microsomes.
2002-03
The tetrahymena ribozyme cleaves a 5'-methylene phosphonate monoester approximately 10(2)-fold faster than a normal phosphate diester: implications for enzyme catalysis of phosphoryl transfer reactions.
2001-09-18
Synthesis and modulation of cytokine production by two new adamantane substituted acyclic desmuramyldipeptide analogs.
2001-07
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:53:55 GMT 2025
Edited
by admin
on Mon Mar 31 19:53:55 GMT 2025
Record UNII
U9X9YBA22W
Record Status Validated (UNII)
Record Version
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Name Type Language
Diethyl phosphite
Systematic Name English
NSC-2665
Preferred Name English
DIETHYL HYDROGEN PHOSPHITE [HSDB]
Common Name English
Code System Code Type Description
DRUG BANK
DB02811
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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HSDB
2591
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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FDA UNII
U9X9YBA22W
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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ECHA (EC/EINECS)
212-091-6
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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PUBCHEM
220224
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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CAS
762-04-9
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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NSC
2665
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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EPA CompTox
DTXSID9041861
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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WIKIPEDIA
Diethylphosphite
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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CHEBI
41962
Created by admin on Mon Mar 31 19:53:55 GMT 2025 , Edited by admin on Mon Mar 31 19:53:55 GMT 2025
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