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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-(3-aminophenyl)-

CCC(=O)Nc1cccc(c1)N Request for Quotation
Chemical Name: Propanamide, N-(3-aminophenyl)-
CAS Number: 22987-10-6
Product Number: AG002LS9(AGN-PC-0JLYC1)
Synonyms:
MDL No:
Molecular Formula: C9H12N2O
Molecular Weight: 164.2044

Identification/Properties

Properties
MP:
92-96 °C(lit.)
BP:
392.028 °C at 760 mmHg
Form:
Solid
Computed Properties
Molecular Weight:
164.208g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
164.095g/mol
Monoisotopic Mass:
164.095g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
159
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(3-Aminophenyl)propionamide, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique chemical properties.One significant application of $name$ in chemical synthesis is as a key building block in the creation of organic compounds with diverse functionalities. Its amide functionality allows for the incorporation of the 3-aminophenyl group into larger molecular structures, providing opportunities for the design and synthesis of complex molecules.Moreover, the presence of the propionamide moiety in $name$ facilitates its use as a protecting group in organic synthesis. By temporarily masking reactive functional groups, propionamide can enable selective reactions and enhance the efficiency of multi-step synthetic pathways.Furthermore, $name$ can serve as a precursor for the synthesis of bioactive compounds and intermediates in the pharmaceutical industry. Through strategic modifications and derivatization, chemists can access a wide range of structurally diverse molecules with potential therapeutic applications.Overall, the versatile nature of N-(3-Aminophenyl)propionamide makes it a valuable tool in chemical synthesis, offering researchers a gateway to the creation of novel compounds with practical applications across various industries.