1. Home
  2. 4-methyl-N-(5-methylpyridin-2-yl)benzamide

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

4-methyl-N-(5-methylpyridin-2-yl)benzamide

Cc1ccc(cc1)C(=O)Nc1ccc(cn1)C Request for Quotation
Chemical Name: 4-methyl-N-(5-methylpyridin-2-yl)benzamide
CAS Number: 349122-64-1
Product Number: AG00C9V4(AGN-PC-0JWRKZ)
Synonyms:
MDL No:
Molecular Formula: C14H14N2O
Molecular Weight: 226.27376

Identification/Properties

Computed Properties
Molecular Weight:
226.279g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
226.111g/mol
Monoisotopic Mass:
226.111g/mol
Topological Polar Surface Area:
42A^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

Request for Quotation

Customer Feedback

Chemical Structure


4-Methyl-N-(5-methyl-2-pyridinyl)benzamide, also known as $name$, serves as a valuable building block in chemical synthesis. This compound is specifically used in organic chemistry reactions to introduce a substituted benzamide group into target molecules. The presence of the methyl and pyridinyl substituents in the structure imparts unique chemical properties, making $name$ a versatile intermediate for the preparation of various functionalized compounds. Researchers and chemists utilize this compound in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. With its strategic placement of functional groups, 4-Methyl-N-(5-methyl-2-pyridinyl)benzamide plays a crucial role in diversifying the molecular structures of complex compounds through efficient synthetic pathways.