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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-N-(2-methylphenyl)-

Cc1ccccc1NC(=O)c1ccccc1N Request for Quotation
Chemical Name: Benzamide, 2-amino-N-(2-methylphenyl)-
CAS Number: 4943-85-5
Product Number: AG00DBL8(AGN-PC-0JVFO5)
Synonyms:
MDL No:
Molecular Formula: C14H14N2O
Molecular Weight: 226.2738

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
226.279g/mol
XLogP3:
3
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:
267
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-N-(o-tolyl)benzamide is a versatile compound widely used in chemical synthesis for its valuable applications. In the field of organic chemistry, this compound serves as a key building block in the preparation of various complex molecules and pharmaceuticals. Its unique structure enables it to participate in a range of reactions, making it a valuable tool for chemists in the design and synthesis of new compounds.One of the primary applications of 2-Amino-N-(o-tolyl)benzamide is as a starting material for the synthesis of heterocyclic compounds. By reacting this compound with appropriate reagents, chemists can introduce diverse functional groups and substitutions to create a variety of heterocycles with different properties and biological activities. This capability makes 2-Amino-N-(o-tolyl)benzamide an essential component in the development of novel drug candidates and other bioactive molecules.Furthermore, 2-Amino-N-(o-tolyl)benzamide can also be utilized in the synthesis of various dyes and pigments. Its chemical properties allow for the modification of its aromatic ring system, leading to the creation of colorful and stable dye molecules. This application is particularly important in industries such as textiles, cosmetics, and materials science, where the creation of vibrant and durable colorants is essential.Overall, the versatile nature of 2-Amino-N-(o-tolyl)benzamide makes it a valuable asset in chemical synthesis, offering chemists the flexibility and control needed to design and create a wide range of organic compounds with diverse applications and functionalities.