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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, 4-amino-N-(2,6-dimethylphenyl)-

O=C(c1ccc(cc1)N)Nc1c(C)cccc1C Request for Quotation
Chemical Name: Benzamide, 4-amino-N-(2,6-dimethylphenyl)-
CAS Number: 787-93-9
Product Number: AG005DHO(AGN-PC-0JKAZ7)
Synonyms:
MDL No:
Molecular Formula: C15H16N2O
Molecular Weight: 240.3003

Identification/Properties

Properties
MP:
220 - 222 °C
Storage:
-10 ℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
240.306g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
240.126g/mol
Monoisotopic Mass:
240.126g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
274
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Amino-N-(2,6-dimethylphenyl)benzamide, a versatile compound in chemical synthesis, serves as a key building block in the preparation of various organic molecules. Its primary application lies in its role as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials.In organic chemistry, 4-Amino-N-(2,6-dimethylphenyl)benzamide acts as a valuable starting material for the creation of heterocyclic compounds, which are widely used in medicinal chemistry. It participates in numerous reactions such as acylation, amidation, and nucleophilic substitution, enabling the efficient formation of complex chemical structures.Furthermore, this compound plays a significant role in the design and development of new drug candidates. By incorporating 4-Amino-N-(2,6-dimethylphenyl)benzamide into a molecule, chemists can modulate the biological activity, metabolic stability, and pharmacokinetic properties of potential drug compounds, thereby enhancing their efficacy and safety profiles.Overall, the strategic utilization of 4-Amino-N-(2,6-dimethylphenyl)benzamide in chemical synthesis empowers researchers to explore innovative pathways for synthesizing bioactive molecules with diverse applications in the fields of medicine, agriculture, and material science.