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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)-

N-(2-Aminoethyl)-4-tert-butyl-2,6-xylylacetamide

NCCNC(=O)Cc1c(C)cc(cc1C)C(C)(C)C Request for Quotation
Chemical Name: N-(2-Aminoethyl)-4-tert-butyl-2,6-xylylacetamide
CAS Number: 94266-17-8
Product Number: AG01CBNS(AGN-PC-0JN7NB)
Synonyms:
MDL No:
Molecular Formula: C16H26N2O
Molecular Weight: 262.39044

Identification/Properties

Computed Properties
Molecular Weight:
262.397g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
262.205g/mol
Monoisotopic Mass:
262.205g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
284
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-Aminoethyl)-4-(1,1-dimethylethyl)-2,6-dimethylbenzeneacetamide, commonly referred to as $name$, serves as a valuable reagent in chemical synthesis processes. This compound is particularly renowned for its role in the formation of complex organic structures by facilitating key reactions.In chemical synthesis, $name$ is utilized as a versatile building block due to its unique chemical properties. Its functional groups enable it to participate in various transformative reactions, contributing to the creation of diverse molecular frameworks. By serving as a crucial intermediate, $name$ aids in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.Furthermore, the presence of the aminoethyl moiety in $name$ offers a site for further functionalization, allowing for the introduction of additional chemical functionalities. This feature enhances the adaptability of $name$ in customizing the desired molecular properties, making it a preferred choice in the synthesis of intricate compounds.Overall, the application of N-(2-Aminoethyl)-4-(1,1-dimethylethyl)-2,6-dimethylbenzeneacetamide in chemical synthesis underscores its significance as a key component in the construction of diverse organic molecules with tailored properties and functions.