ethyl benzo[b]thiophene-7-carboxylate|959632-57-6,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)-

ethyl benzo[b]thiophene-7-carboxylate

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Chemical Name:	ethyl benzo[b]thiophene-7-carboxylate
CAS Number:	959632-57-6
Product Number:	AG005WGE(AGN-PC-086DM7)
Synonyms:
MDL No:
Molecular Formula:	C11H10O2S
Molecular Weight:	206.2609

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Keep in dry area;2-8℃;

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Chemical Structure

Ethyl benzo[b]thiophene-7-carboxylate is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it valuable in various organic reactions.One common application of ethyl benzo[b]thiophene-7-carboxylate is its role as a building block in the synthesis of complex organic molecules. It serves as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and materials with specific functionalities. By undergoing various chemical transformations, ethyl benzo[b]thiophene-7-carboxylate can be modified to introduce specific functional groups or structural motifs into the final product.Furthermore, ethyl benzo[b]thiophene-7-carboxylate is often used as a precursor in the development of novel materials with desired properties. Its incorporation into polymer chains or organic frameworks can impart enhanced stability, reactivity, or other characteristics important for specific applications.Overall, the versatility of ethyl benzo[b]thiophene-7-carboxylate in chemical synthesis makes it a valuable tool for organic chemists seeking to design and access new molecules with tailored properties and functions.