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Home Other Building Blocks GLUFOSINATE-N-ACETYL

GLUFOSINATE-N-ACETYL

CAS No.:
73634-73-8
Catalog Number:
AG00FAV3
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG00FAV3
Chemical Name:
GLUFOSINATE-N-ACETYL
CAS Number:
73634-73-8
MDL Number:
MFCD08273844
IUPAC Name:
2-acetamido-4-[hydroxy(methyl)phosphoryl]butanoic acid
InChI:
InChI=1S/C7H14NO5P/c1-5(9)8-6(7(10)11)3-4-14(2,12)13/h6H,3-4H2,1-2H3,(H,8,9)(H,10,11)(H,12,13)
InChI Key:
VZVQOWUYAAWBCP-UHFFFAOYSA-N
Properties
Complexity:
277  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
223.061g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
223.165g/mol
Monoisotopic Mass:
223.061g/mol
Rotatable Bond Count:
5  
Topological Polar Surface Area:
104A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.8  
Literature
Title Journal
Distribution and metabolism of D/L-, L- and D-glufosinate in transgenic, glufosinate-tolerant crops of maize (Zea mays L ssp mays) and oilseed rape (Brassica napus L var napus). Pest management science 20040701
Development of antibodies for the detection of N-acetyl-glufosinate. Journal of agricultural and food chemistry 20031105
Metabolism of the herbicide glufosinate-ammonium in plant cell cultures of transgenic (rhizomania-resistant) and non-transgenic sugarbeet (Beta vulgaris), carrot (Daucus carota), purple foxglove (Digitalis purpurea) and thorn apple (Datura stramonium). Pest management science 20010101
Phosphinothricin-tripeptide synthetases from Streptomyces viridochromogenes. Biochemistry 19980210
Properties