1. Home
  2. 1H-Indole-3-ethanamine, 6-bromo-

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-ethanamine, 6-bromo-

NCCc1c[nH]c2c1ccc(c2)Br Request for Quotation
Chemical Name: 1H-Indole-3-ethanamine, 6-bromo-
CAS Number: 96624-18-9
Product Number: AG00IJUE(AGN-PC-0JNG1W)
Synonyms:
MDL No:
Molecular Formula: C10H11BrN2
Molecular Weight: 239.1117

Identification/Properties

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The application of 2-(6-Bromo-1H-indol-3-yl)ethanamine in chemical synthesis lies in its versatile reactivity as a key building block. This compound serves as a valuable intermediate in the synthesis of various biologically active molecules, pharmaceuticals, and agrochemicals. As a primary amine with a bromoindole moiety, it allows for selective functionalization and elaboration through various synthetic transformations such as cross-coupling reactions, nucleophilic substitutions, and reductive aminations. Additionally, the presence of the indole ring confers unique aromatic and electron-rich properties that enable the diversification of chemical structures. The strategic incorporation of 2-(6-Bromo-1H-indol-3-yl)ethanamine into synthetic routes offers chemists a powerful tool to access complex molecular architectures and explore new avenues in drug discovery and material science.