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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)-

Benzo[b]thiophene-2-carboxylic acid, 6-methoxy-, methyl ester

COc1ccc2c(c1)sc(c2)C(=O)OC Request for Quotation
Chemical Name: Benzo[b]thiophene-2-carboxylic acid, 6-methoxy-, methyl ester
CAS Number: 550998-58-8
Product Number: AG00DI63(AGN-PC-09TQ56)
Synonyms:
MDL No:
Molecular Formula: C11H10O3S
Molecular Weight: 222.2603

Identification/Properties

Properties
BP:
345°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 6-methoxybenzo[b]thiophene-2-carboxylate is a versatile compound commonly used in chemical synthesis as a key building block for organic reactions. This compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity. Its ester group, methoxybenzene moiety, and thiophene ring make it a valuable starting material for the creation of more complex molecules. One of the primary applications of Methyl 6-methoxybenzo[b]thiophene-2-carboxylate is in the synthesis of heterocyclic compounds, which are important in drug discovery and development. Additionally, this compound can be utilized in the preparation of functional materials such as polymers and liquid crystals. Its presence in the chemical toolbox enables chemists to access a wide range of molecular structures with diverse properties, making it an indispensable component in modern organic synthesis strategies.