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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)-

2H-Indol-2-one, 3-(2-aminoethyl)-1,3-dihydro-

NCCC1C(=O)Nc2c1cccc2 Request for Quotation
Chemical Name: 2H-Indol-2-one, 3-(2-aminoethyl)-1,3-dihydro-
CAS Number: 60716-71-4
Product Number: AG00EDDC(AGN-PC-0JKFOH)
Synonyms:
MDL No:
Molecular Formula: C10H12N2O
Molecular Weight: 176.2151

Identification/Properties

Properties
Storage:
2-8℃;Light sensitive;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2H-Indol-2-one, 3-(2-aminoethyl)-1,3-dihydro- is a versatile chemical compound commonly utilized in chemical synthesis processes. Known for its reactivity and structural properties, this compound is highly valued for its role in various organic reactions. One of the key applications of 2H-Indol-2-one, 3-(2-aminoethyl)-1,3-dihydro- in chemical synthesis is as a crucial intermediate in the formation of biologically active compounds. Its presence in synthetic schemes enables the introduction of key functional groups and the modification of molecular structures to generate diverse chemical entities with potential pharmacological activities. Additionally, owing to its unique composition, this compound serves as a valuable building block in the creation of novel molecules for medicinal chemistry research and drug development efforts. Its strategic placement within synthetic pathways allows for the controlled manipulation of chemical reactivity, enabling the synthesis of complex organic molecules with enhanced properties and functionalities. The utilization of 2H-Indol-2-one, 3-(2-aminoethyl)-1,3-dihydro- in chemical synthesis showcases its significance as a fundamental component in the creation of advanced materials and bioactive compounds, highlighting its pivotal role in the field of organic chemistry.