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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)-

potassium;2-carbamoyl-3-nitrobenzoate

[O-]C(=O)c1cccc(c1C(=O)N)[N+](=O)[O-].[K+] Request for Quotation
Chemical Name: potassium;2-carbamoyl-3-nitrobenzoate
CAS Number: 943522-94-9
Product Number: AG005Z10(AGN-PC-07Y48P)
Synonyms:
MDL No:
Molecular Formula: C8H5KN2O5
Molecular Weight: 248.2340

Identification/Properties

Computed Properties
Molecular Weight:
248.235g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
247.984g/mol
Monoisotopic Mass:
247.984g/mol
Topological Polar Surface Area:
129A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
292
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Aminocarbonyl)-3-nitrobenzoic Acid Potassium Salt is a versatile compound widely utilized in chemical synthesis as a key reagent. In organic chemistry, it serves as an important building block for the preparation of various pharmaceuticals, agrochemicals, and functional materials. This compound's unique structure allows it to participate in a range of reactions, including condensation, acylation, and nucleophilic substitution, enabling the efficient synthesis of complex molecules. Its water-soluble nature also makes it particularly suitable for aqueous-based reactions, offering flexibility in reaction conditions. Additionally, the presence of both an amino group and a nitro group in the molecule imparts distinct properties that can be leveraged in the design of novel compounds.