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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)-

2-Thiophenecarboxylic acid, tetrahydro-4-methyl-3-oxo-, methyl ester

COC(=O)C1SCC(C1=O)C Request for Quotation
Chemical Name: 2-Thiophenecarboxylic acid, tetrahydro-4-methyl-3-oxo-, methyl ester
CAS Number: 2689-70-5
Product Number: AG00C12M(AGN-PC-0N598S)
Synonyms:
MDL No:
Molecular Formula: C7H10O3S
Molecular Weight: 174.2175

Identification/Properties

Properties
BP:
254°C
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 4-methyl-3-oxotetrahydrothiophene-2-carboxylate is a versatile compound commonly used in chemical synthesis for its diverse applications. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural properties and reactivity. In chemical synthesis, Methyl 4-methyl-3-oxotetrahydrothiophene-2-carboxylate can function as a starting material for the production of complex organic molecules through various reactions such as esterification, acylation, and nucleophilic substitutions. Its presence in the synthesis process allows for the introduction of specific functional groups and modifications, leading to the formation of novel compounds with desirable properties. Additionally, the incorporation of Methyl 4-methyl-3-oxotetrahydrothiophene-2-carboxylate in chemical reactions enables chemists to access a wide range of structural motifs and molecular diversity, making it an essential component in the toolkit of synthetic chemists.