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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)-

1H-Indole-2-carboxylic acid, 4-bromo-5-methoxy-, ethyl ester

CCOC(=O)c1cc2c([nH]1)ccc(c2Br)OC Request for Quotation
Chemical Name: 1H-Indole-2-carboxylic acid, 4-bromo-5-methoxy-, ethyl ester
CAS Number: 30933-69-8
Product Number: AG0031P1(AGN-PC-009K9M)
Synonyms:
MDL No:
Molecular Formula: C12H12BrNO3
Molecular Weight: 298.1326

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 4-Bromo-5-methoxy-1H-indole-2-carboxylate is a key intermediate commonly used in the field of organic chemistry. This compound plays a crucial role in chemical synthesis, particularly in the creation of various indole derivatives. Its unique structure makes it a valuable building block for designing new pharmaceuticals, agrochemicals, and other biologically active compounds.In organic synthesis, Ethyl 4-Bromo-5-methoxy-1H-indole-2-carboxylate serves as a versatile starting material for the preparation of complex molecules with diverse functionalities. Its presence in the reaction sequence allows for the introduction of specific functional groups at strategic positions, enabling chemists to tailor the properties of the final product according to desired specifications.Furthermore, the reactivity of Ethyl 4-Bromo-5-methoxy-1H-indole-2-carboxylate can be harnessed to facilitate transformations like substitution, addition, and cyclization reactions. By leveraging the regioselectivity and reactivity of this substrate, chemists can access a wide range of molecular scaffolds and structural motifs that are essential for drug discovery, material science, and other chemical research endeavors.