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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, N-(2-aminoethyl)-

NCCNC(=O)CC Request for Quotation
Chemical Name: Propanamide, N-(2-aminoethyl)-
CAS Number: 925-58-6
Product Number: AG0064FC(AGN-PC-0LD4DH)
Synonyms:
MDL No:
Molecular Formula: C5H12N2O
Molecular Weight: 116.1616

Identification/Properties

Computed Properties
Molecular Weight:
116.164g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
116.095g/mol
Monoisotopic Mass:
116.095g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
72.8
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)propionamide, also known as AEB, serves as a versatile building block in chemical synthesis. Its primary application lies in the synthesis of bioactive compounds, pharmaceuticals, and agrochemicals. AEB can be utilized as a key intermediate in the production of various organic compounds through its ability to participate in a wide range of chemical reactions, such as amidation, alkylation, and cyclization. In pharmaceutical research and development, AEB is often employed for the creation of new drug candidates due to its structural flexibility and diverse functional groups. Additionally, AEB plays a crucial role in the design and synthesis of novel materials with tailored properties, making it a valuable tool in the realm of materials science. Its compatibility with various functional groups and its ability to undergo selective modifications make N-(2-Aminoethyl)propionamide a preferred choice for chemists seeking to diversify their chemical synthesis strategies.