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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, N-(2-aminophenyl)-4-methyl-

Cc1ccc(cc1)C(=O)Nc1ccccc1N Request for Quotation
Chemical Name: Benzamide, N-(2-aminophenyl)-4-methyl-
CAS Number: 71255-53-3
Product Number: AG00FUQ3(AGN-PC-0L7IH3)
Synonyms:
MDL No: MFCD00447039
Molecular Formula: C14H14N2O
Molecular Weight: 226.2738

Identification/Properties

Computed Properties
Molecular Weight:
226.279g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
226.111g/mol
Monoisotopic Mass:
226.111g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
259
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


N-(2-Aminophenyl)-4-methylbenzamide is a versatile chemical compound that finds widespread application in organic synthesis procedures. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, N-(2-Aminophenyl)-4-methylbenzamide acts as a key intermediate in the creation of structurally complex molecules with desired biological or chemical properties. Its unique structure and reactivity make it an essential component in the development of novel compounds with potential applications in medicine, agriculture, and materials science. By incorporating N-(2-Aminophenyl)-4-methylbenzamide into synthetic routes, chemists can access a diverse range of molecular architectures, enabling the discovery of innovative products and solutions.