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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)-

Benzamide, 2-amino-3-nitro-

NC(=O)c1cccc(c1N)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzamide, 2-amino-3-nitro-
CAS Number: 313279-12-8
Product Number: AG00C11I(AGN-PC-0NAQC6)
Synonyms:
MDL No:
Molecular Formula: C7H7N3O3
Molecular Weight: 181.1488

Identification/Properties

Computed Properties
Molecular Weight:
181.151g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
181.049g/mol
Monoisotopic Mass:
181.049g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
226
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-3-nitrobenzamide, also known as ANBA, is a versatile compound widely utilized in chemical synthesis as a key building block for various organic reactions and transformations. This compound plays a crucial role in the pharmaceutical and materials industries due to its unique chemical properties and reactivity. In chemical synthesis, 2-Amino-3-nitrobenzamide is commonly employed as a precursor for the synthesis of biologically active molecules, pharmaceutical intermediates, and functional materials. Its amino and nitro functional groups make it a valuable starting material for the construction of diverse chemical structures via various synthetic routes including reductive amination, nucleophilic substitution, and transition metal-catalyzed reactions. Additionally, 2-Amino-3-nitrobenzamide can serve as a building block for the introduction of amide, amine, or nitro groups into target molecules, enabling the modification and optimization of chemical properties for specific applications. Due to its synthetic versatility and compatibility with a wide range of chemical reactions, 2-Amino-3-nitrobenzamide is an indispensable tool in the hands of organic chemists for the efficient and controllable synthesis of complex molecular structures with tailored properties.