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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 4-fluoro-7-nitro-1H-indole-2-carboxylate

CCOC(=O)c1cc2c([nH]1)c(ccc2F)[N+](=O)[O-] Request for Quotation
Chemical Name: ethyl 4-fluoro-7-nitro-1H-indole-2-carboxylate
CAS Number: 913287-14-6
Product Number: AG00IGLE(AGN-PC-09SIW2)
Synonyms:
MDL No:
Molecular Formula: C11H9FN2O4
Molecular Weight: 252.1985632

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 4-fluoro-7-nitro-1H-indole-2-carboxylate is a key compound in chemical synthesis, often utilized as a versatile building block in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. This compound serves as a valuable intermediate in the synthesis of various biologically active molecules due to its unique structural properties.In chemical synthesis, Ethyl 4-fluoro-7-nitro-1H-indole-2-carboxylate can be employed in the formation of complex heterocyclic compounds through diverse synthetic routes. Its presence enables the introduction of functional groups and modifications that are crucial for enhancing the desired properties of the final product. Additionally, this compound can participate in key reactions such as nucleophilic substitutions, cyclizations, and cross-coupling reactions, expanding its utility in the synthesis of diverse chemical entities.Furthermore, Ethyl 4-fluoro-7-nitro-1H-indole-2-carboxylate's structural features make it a valuable precursor for the creation of compounds with potential therapeutic applications, making it a valuable asset in medicinal chemistry research. Its ability to undergo a variety of transformations under controlled conditions highlights its significance in the design and development of novel molecules with targeted biological activities.Overall, the versatility and reactivity of Ethyl 4-fluoro-7-nitro-1H-indole-2-carboxylate make it a valuable component in the arsenal of synthetic chemists seeking to access a diverse array of compounds with tailored properties for various scientific and industrial applications.