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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)-

ethyl 2,3-dihydro-1H-indole-6-carboxylate

CCOC(=O)c1ccc2c(c1)NCC2 Request for Quotation
Chemical Name: ethyl 2,3-dihydro-1H-indole-6-carboxylate
CAS Number: 350683-40-8
Product Number: AG00CIR9(AGN-PC-0NP8JF)
Synonyms:
MDL No:
Molecular Formula: C11H13NO2
Molecular Weight: 191.2264

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of Ethyl indoline-6-carboxylate in chemical synthesis lies in its versatile nature as a chemical building block. This compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Ethyl indoline-6-carboxylate can participate in a range of organic reactions, including condensation, alkylation, and cyclization processes, allowing for the functionalization and modification of its structure to tailor its properties for specific applications. By incorporating Ethyl indoline-6-carboxylate into synthetic routes, chemists can access complex molecular scaffolds and achieve the strategic assembly of target molecules with desired biological or chemical activities.