Details
Stereochemistry | ACHIRAL |
Molecular Formula | C2H7O3P |
Molecular Weight | 110.049 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COP(=O)OC
InChI
InChIKey=HZCDANOFLILNSA-UHFFFAOYSA-N
InChI=1S/C2H7O3P/c1-4-6(3)5-2/h6H,1-2H3
Molecular Formula | C2H7O3P |
Molecular Weight | 110.049 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Cytosolic acidification as a signal mediating hyperosmotic stress responses in Dictyostelium discoideum. | 2001 |
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Dealkylation of phosphonate esters with chlorotrimethylsilane. | 2001 Apr-Jul |
|
Structure of hybrid backbone methylphosphonate DNA heteroduplexes: effect of R and S stereochemistry. | 2002 Jan 22 |
|
Stereoselectivity in deoxygenation of 5-hydroxy-5-phosphinyl-hexofuranoses (alpha-hydroxyphosphonates). | 2003 Jul 29 |
|
Biodistribution and pharmacokinetics of variously molecular sized 117mSn(II)-polyethyleneiminomethyl phosphonate complexes in the normal primate model as potential selective therapeutic bone agents. | 2004 |
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Theoretical study of the spin trapping of hydroxyl radical by cyclic nitrones: a density functional theory approach. | 2004 Feb 18 |
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Electrostatic interactions and the folding of the four-way DNA junction: analysis by selective methyl phosphonate substitution. | 2004 Oct 29 |
|
Atmospheric chemistry of dimethyl phosphonate, dimethyl methylphosphonate, and dimethyl ethylphosphonate. | 2005 Dec 29 |
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Stereospecific effects determine the structure of a four-way DNA junction. | 2005 Feb |
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Multidimensional analytical method based on binary phase shaping of femtosecond pulses. | 2005 Mar 24 |
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Does phosphoryl protonation occurs in aqueous phosphoesters solutions. | 2005 Nov |
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Ion-pair solid-phase extraction and gas chromatography-mass spectrometric determination of acidic hydrolysis products of chemical warfare agents from aqueous samples. | 2006 Sep 29 |
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Femtosecond pulse shaping adds a new dimension to mass spectrometry. | 2007 Jul 1 |
|
Structural diversity within the mononuclear and binuclear active sites of N-acetyl-D-glucosamine-6-phosphate deacetylase. | 2007 Jul 10 |
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A solid-state NMR study of hydrogen-bonding networks and ion dynamics in benzimidazole salts. | 2007 May 24 |
|
Screening organophosphorus nerve agent degradation products in pesticide mixtures by GC-ICPMS. | 2007 Oct |
|
C-bis-pivot lariat ethers: synthesis and spectral investigations on new 15- and 17-membered coronands containing dimethoxyphosphoryl groups. | 2008 Aug |
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Snapshots of catalysis in the E1 subunit of the pyruvate dehydrogenase multienzyme complex. | 2008 Dec 10 |
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Rate constants for the gas-phase reactions of OH radicals with dimethyl phosphonate over the temperature range of 278-351 K and for a series of other organophosphorus compounds at approximately 280 K. | 2008 May 29 |
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Efficient second strand cleavage during Holliday junction resolution by RuvC requires both increased junction flexibility and an exposed 5' phosphate. | 2009 |
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Response of cytoplasmic pH to anoxia in plant tissues with altered activities of fermentation enzymes: application of methyl phosphonate as an NMR pH probe. | 2009 Jan |
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Handling within run retention time shifts in two-dimensional chromatography data using shift correction and modeling. | 2009 May 1 |
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Functional identification of incorrectly annotated prolidases from the amidohydrolase superfamily of enzymes. | 2009 May 5 |
|
Solvent-free synthesis of pyrimidine nucleoside-aminophosphonate hybrids and their biological activity evaluation. | 2010 Aug |
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Detection of a nerve agent simulant using single-walled carbon nanotube networks: dimethyl-methyl-phosphonate. | 2010 Dec 10 |
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Plasma chemical degradation of phosphorous-containing warfare agents simulants. | 2010 Mar 15 |
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Removal of glyphosate in neutralization liquor from the glycine-dimethylphosphit process by nanofiltration. | 2010 Sep 15 |
|
Identification of thioaptamer ligand against E-selectin: potential application for inflamed vasculature targeting. | 2010 Sep 30 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Jun 26 11:26:45 UTC 2021
by
admin
on
Sat Jun 26 11:26:45 UTC 2021
|
Record UNII |
ST4TBO000H
|
Record Status |
Validated (UNII)
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Record Version |
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2593
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13361
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212-783-8
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868-85-9
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C047356
Created by
admin on Sat Jun 26 11:26:45 UTC 2021 , Edited by admin on Sat Jun 26 11:26:45 UTC 2021
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868-85-9
Created by
admin on Sat Jun 26 11:26:45 UTC 2021 , Edited by admin on Sat Jun 26 11:26:45 UTC 2021
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ST4TBO000H
Created by
admin on Sat Jun 26 11:26:45 UTC 2021 , Edited by admin on Sat Jun 26 11:26:45 UTC 2021
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PRIMARY |