1. Home
  2. 1H-Indole-3-propanamide

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1H-Indole-3-propanamide

NC(=O)CCc1c[nH]c2c1cccc2 Request for Quotation
Chemical Name: 1H-Indole-3-propanamide
CAS Number: 5814-93-7
Product Number: AG00EBFE(AGN-PC-0JQ9WZ)
Synonyms:
MDL No:
Molecular Formula: C11H12N2O
Molecular Weight: 188.2258

Identification/Properties

Properties
MP:
169-170 °C
BP:
487.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
188.23g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
188.095g/mol
Monoisotopic Mass:
188.095g/mol
Topological Polar Surface Area:
58.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
217
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

Request for Quotation

Customer Feedback

Chemical Structure


3-(1H-Indol-3-yl)propanamide is a versatile compound widely utilized in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and organic materials. This compound serves as a crucial building block in the synthesis of biologically active molecules, particularly within the field of medicinal chemistry. Its unique structure containing an indole ring and an amide group provides a platform for the creation of diverse chemical structures with potentially valuable biological properties.In chemical synthesis, 3-(1H-Indol-3-yl)propanamide can be employed in the development of novel drug candidates, as indole derivatives have exhibited various pharmacological activities such as anti-inflammatory, anti-cancer, and antimicrobial properties. By strategically modifying the chemical structure around the indole moiety, researchers can fine-tune the biological properties of the resulting molecules, aiming to enhance efficacy and reduce side effects.Furthermore, 3-(1H-Indol-3-yl)propanamide can also be utilized in the synthesis of natural products, dyes, and functional materials, showcasing its versatility in organic chemistry applications beyond the pharmaceutical industry. Its role as a synthetic intermediate enables chemists to access complex molecular architectures efficiently, facilitating the discovery and development of new compounds with potential applications in diverse fields.Overall, the application of 3-(1H-Indol-3-yl)propanamide in chemical synthesis underlines its significance as a valuable building block for creating molecular diversity and exploring the biological activities of indole-containing compounds.