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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)-

Butanamide, 2-[(5-fluoro-2,4-dinitrophenyl)amino]-3-methyl-, (S)-

CC([C@@H](C(=O)N)Nc1cc(F)c(cc1[N+](=O)[O-])[N+](=O)[O-])C Request for Quotation
Chemical Name: Butanamide, 2-[(5-fluoro-2,4-dinitrophenyl)amino]-3-methyl-, (S)-
CAS Number: 132679-61-9
Product Number: AG0010YX(AGN-PC-0O12J1)
Synonyms:
MDL No:
Molecular Formula: C11H13FN4O5
Molecular Weight: 300.2431

Identification/Properties

Computed Properties
Molecular Weight:
300.246g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
4
Exact Mass:
300.087g/mol
Monoisotopic Mass:
300.087g/mol
Topological Polar Surface Area:
147A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
422
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, (S)-2-((5-Fluoro-2,4-dinitrophenyl)amino)-3-methylbutanamide serves as a versatile and valuable building block for a range of synthetic pathways. This compound can be utilized as a key intermediate in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structural properties. By incorporating this compound into synthetic routes, chemists can access new opportunities for the development of diverse molecular structures with precise stereochemical control. The application of (S)-2-((5-Fluoro-2,4-dinitrophenyl)amino)-3-methylbutanamide enables the synthesis of complex molecules with enhanced biological activities, making it an essential component in the realm of modern organic chemistry.