Home Other Building Blocks 3-Amino-3-oxopropanoic acid

3-Amino-3-oxopropanoic acid

CAS No.:
2345-56-4
Catalog Number:
AG002NA1
Molecular Formula:
C3H5NO3
Molecular Weight:
103.0767
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$358
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Product Description
Catalog Number:
AG002NA1
Chemical Name:
3-Amino-3-oxopropanoic acid
CAS Number:
2345-56-4
Molecular Formula:
C3H5NO3
Molecular Weight:
103.0767
MDL Number:
MFCD00154605
IUPAC Name:
3-amino-3-oxopropanoic acid
InChI:
InChI=1S/C3H5NO3/c4-2(5)1-3(6)7/h1H2,(H2,4,5)(H,6,7)
InChI Key:
CGJMROBVSBIBKP-UHFFFAOYSA-N
SMILES:
NC(=O)CC(=O)O
EC Number:
219-069-5
UNII:
30H7L7X07N
NSC Number:
1812
Properties
Complexity:
98.4  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
103.027g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
103.077g/mol
Monoisotopic Mass:
103.027g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
80.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.5  
Literature
Title Journal
Discovery of novel indane derivatives as liver-selective thyroid hormone receptor β (TRβ) agonists for the treatment of dyslipidemia. Bioorganic & medicinal chemistry 20120601
Design, synthesis and inhibition activity of a novel cyclic enediyne amino acid conjugates against MPtpA. Bioorganic & medicinal chemistry 20110515
Substituted aryl malonamates as new serine beta-lactamase substrates: structure-activity studies. Bioorganic & medicinal chemistry 20100101
The highly enantioselective phase-transfer catalytic mono-alkylation of malonamic esters. Chemical communications (Cambridge, England) 20090221
Arg-158 is critical in both binding the substrate and stabilizing the transition-state oxyanion for the enzymatic reaction of malonamidase E2. The Journal of biological chemistry 20061229
Microbial transformation products of benzoxazolinone and benzoxazinone allelochemicals--a review. Chemosphere 20040201
Practical synthesis of optically active alpha,alpha-disubstituted malonamic acids through asymmetric hydrolysis of malonamide derivatives with Rhodococcus sp. CGMCC 0497. The Journal of organic chemistry 20030321
Identification of fonofos metabolites in Latuca sativa, Beta vulgaris, and Triticum aestivum by packed capillary flow fast atom bombardment tandem mass spectrometry. Journal of agricultural and food chemistry 20020327
Crystallization and preliminary X-ray crystallographic analysis of malonamidase E2, an amidase signature family member. Acta crystallographica. Section D, Biological crystallography 20020301
Properties