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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-(1,1-dimethylethyl)-2-methyl-

O=C(c1ccccc1C)NC(C)(C)C Request for Quotation
Chemical Name: Benzamide, N-(1,1-dimethylethyl)-2-methyl-
CAS Number: 104847-07-6
Product Number: AG003TCR(AGN-PC-0LM4JS)
Synonyms:
MDL No:
Molecular Formula: C12H17NO
Molecular Weight: 191.2695

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
191.274g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
191.131g/mol
Monoisotopic Mass:
191.131g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
205
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-(tert-Butyl)-2-methylbenzamide is a versatile compound that finds wide application in chemical synthesis processes. As a key building block in organic chemistry, this compound serves as a crucial intermediate in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structural properties enable it to participate in a range of reactions, including amidation, nucleophilic substitution, and palladium-catalyzed cross-coupling reactions.In the realm of drug discovery and development, N-(tert-Butyl)-2-methylbenzamide plays a significant role as a precursor for the synthesis of biologically active compounds. Its presence in the molecular structure of many pharmaceutical agents contributes to their enhanced pharmacological properties and improved efficacy. Additionally, this compound serves as a valuable tool in the study of structure-activity relationships, aiding researchers in the design and optimization of novel drug candidates.Beyond the pharmaceutical industry, N-(tert-Butyl)-2-methylbenzamide is employed in the synthesis of specialty chemicals with diverse applications. Its versatile reactivity and compatibility with a range of functional groups make it a sought-after reagent for the construction of complex molecular frameworks. By facilitating key bond formations and functional group manipulations, this compound enables chemists to access a wide array of structurally intricate molecules with tailored properties.Overall, N-(tert-Butyl)-2-methylbenzamide stands as a vital component in modern chemical synthesis, driving innovation and discovery across various sectors. Its strategic role as a versatile building block underscores its importance in the advancement of synthetic methodologies and the creation of novel chemical entities.