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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)-

Propanamide, 3-amino-N-(phenylmethyl)-

NCCC(=O)NCc1ccccc1 Request for Quotation
Chemical Name: Propanamide, 3-amino-N-(phenylmethyl)-
CAS Number: 64018-20-8
Product Number: AG00ELCZ(AGN-PC-0JODSG)
Synonyms:
MDL No:
Molecular Formula: C10H14N2O
Molecular Weight: 178.23096

Identification/Properties

Computed Properties
Molecular Weight:
178.235g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
178.111g/mol
Monoisotopic Mass:
178.111g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
153
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


3-Amino-n-benzylpropanamide, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. One of the key applications of 3-Amino-n-benzylpropanamide in chemical synthesis is as a key intermediate in the preparation of various pharmaceutical compounds. Its structural features make it an essential building block for the synthesis of biologically active molecules, including potential drug candidates.Furthermore, 3-Amino-n-benzylpropanamide serves as a valuable tool in the design and development of novel organic compounds, particularly in the field of medicinal chemistry. Its ability to undergo various transformations and reactions allows chemists to explore different chemical pathways and optimize the synthesis of target molecules. In addition, the presence of the amino group in 3-Amino-n-benzylpropanamide enables further functionalization, leading to the generation of diverse chemical structures with specific properties.In summary, the application of 3-Amino-n-benzylpropanamide in chemical synthesis extends to the creation of pharmaceuticals and other complex organic molecules, showcasing its significance in the realm of modern chemistry and drug discovery.