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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

5-[2-(methylamino)-5-nitroanilino]-5-oxopentanoic acid

CNc1ccc(cc1NC(=O)CCCC(=O)O)[N+](=O)[O-] Request for Quotation
Chemical Name: 5-[2-(methylamino)-5-nitroanilino]-5-oxopentanoic acid
CAS Number: 91644-13-2
Product Number: AG006RJL(AGN-PC-00KTPS)
Synonyms:
MDL No:
Molecular Formula: C12H15N3O5
Molecular Weight: 281.2646

Identification/Properties

Properties
MP:
170.5-171.5℃(Solv: ethanol (64-17-5))
BP:
582.1°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
281.268g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
6
Exact Mass:
281.101g/mol
Monoisotopic Mass:
281.101g/mol
Topological Polar Surface Area:
124A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
369
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-((2-(Methylamino)-5-nitrophenyl)amino)-5-oxopentanoic acid, also known as $name$, serves as a valuable building block in chemical synthesis, particularly in the field of pharmaceuticals. Due to its unique molecular structure, this compound plays a crucial role in the creation of various pharmaceutical agents and drug intermediates. Its functional groups offer versatility in forming key connections during synthetic processes, enabling the development of potent and selective drug molecules. Additionally, $name$ exhibits favorable reactivity and compatibility with numerous chemical reactions, making it an indispensable component in the synthesis of complex organic compounds. In pharmaceutical research and development, the strategic incorporation of $name$ facilitates the efficient production of novel therapeutic compounds with enhanced pharmacological properties. Through its contribution to chemical synthesis, $name$ contributes significantly to the advancement of medicinal chemistry and the discovery of innovative drug candidates.