Home Nitros 4-nitrophenyl 2-propylmethylphosphonate

4-nitrophenyl 2-propylmethylphosphonate

CAS No.:
3735-97-5
Catalog Number:
AG00CZZO
Molecular Formula:
Molecular Weight:
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
Product Description
Catalog Number:
AG00CZZO
Chemical Name:
4-nitrophenyl 2-propylmethylphosphonate
CAS Number:
3735-97-5
MDL Number:
MFCD01099252
IUPAC Name:
1-[methyl(propan-2-yloxy)phosphoryl]oxy-4-nitrobenzene
InChI:
InChI=1S/C10H14NO5P/c1-8(2)15-17(3,14)16-10-6-4-9(5-7-10)11(12)13/h4-8H,1-3H3
InChI Key:
YSHVIWJFWCEDSQ-UHFFFAOYSA-N
Properties
Complexity:
306  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
259.061g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
259.198g/mol
Monoisotopic Mass:
259.061g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
81.4A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
1.9  
Literature
Title Journal
Novel substituted phenoxyalkyl pyridinium oximes enhance survival and attenuate seizure-like behavior of rats receiving lethal levels of nerve agent surrogates. Toxicology 20160102
The effect of PON1 enhancers on reducing acetylcholinesterase inhibition following organophosphate anticholinesterase exposure in rats. Toxicology 20151002
Novel nucleophiles enhance the human serum paraoxonase 1 (PON1)-mediated detoxication of organophosphates. Toxicological sciences : an official journal of the Society of Toxicology 20150101
Synthesis and in vitro and in vivo inhibition potencies of highly relevant nerve agent surrogates. Toxicological sciences : an official journal of the Society of Toxicology 20120401
Asymmetric fluorogenic organophosphates for the development of active organophosphate hydrolases with reversed stereoselectivity. Toxicology 20070420
New safe method for preparation of sarin-exposed human erythrocytes acetylcholinesterase using non-toxic and stable sarin analogue isopropyl p-nitrophenyl methylphosphonate and its application to evaluation of nerve agent antidotes. Pharmaceutical research 20061201
Enhanced stereoselective hydrolysis of toxic organophosphates by directly evolved variants of mammalian serum paraoxonase. The FEBS journal 20060501
Organophosphate nerve agent toxicity in Hydra attenuata. Chemical research in toxicology 20030801
Stereoselective detoxification of chiral sarin and soman analogues by phosphotriesterase. Bioorganic & medicinal chemistry 20010801
Short, strong hydrogen bonds at the active site of human acetylcholinesterase: proton NMR studies. Biochemistry 20010515
Properties