2-(1H-indol-4-yloxy)ethanamine;hydrochloride|91374-26-4,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

2-(1H-indol-4-yloxy)ethanamine;hydrochloride

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Chemical Name:	2-(1H-indol-4-yloxy)ethanamine;hydrochloride
CAS Number:	91374-26-4
Product Number:	AG00GUPS(AGN-PC-03NCHC)
Synonyms:
MDL No:
Molecular Formula:	C10H13ClN2O
Molecular Weight:	212.6760

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Chemical Structure

The chemical compound 2H-Indol-2-one, 4-(2-aminoethyl)-1,3-dihydro-, hydrochloride (1:1) serves as a versatile reagent in chemical synthesis procedures. Its functional groups enable it to participate in various reactions, making it a valuable building block for the creation of complex organic molecules. Through processes like nucleophilic substitution, acylation, and condensation, this compound can be used to introduce specific functionalities or structural motifs into target molecules. Its hydrochloride form provides enhanced solubility in aqueous solutions, facilitating its use in reactions that require water-based environments. Additionally, the compound's stability under typical synthesis conditions makes it a reliable choice for researchers and chemists alike.