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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)-

2,3-Thiophenedicarboxylic acid, 5-methyl-

Cc1cc(c(s1)C(=O)O)C(=O)O Request for Quotation
Chemical Name: 2,3-Thiophenedicarboxylic acid, 5-methyl-
CAS Number: 46029-22-5
Product Number: AG003MWM(AGN-PC-04UYPU)
Synonyms:
MDL No: MFCD14705596
Molecular Formula: C7H6O4S
Molecular Weight: 186.1851

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
186.181g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
185.999g/mol
Monoisotopic Mass:
185.999g/mol
Topological Polar Surface Area:
103A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
216
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methylthiophene-2,3-dicarboxylic acid serves as a valuable building block in organic synthesis, particularly in the field of medicinal chemistry. It is commonly utilized as a key intermediate in the construction of various pharmaceutical compounds due to its versatile reactivity and unique structural properties. The presence of both a thiophene ring and carboxylic acid functional groups in its molecular structure allows for the formation of diverse chemical bonds and enables the introduction of desired functionalities through targeted transformations. This compound can be employed in the synthesis of biologically active molecules, such as potential drug candidates and pharmacological intermediates, by serving as a starting material for the introduction of specific substituents or structural motifs. Additionally, its incorporation into complex molecular frameworks can lead to enhanced biological activities or improved pharmacokinetic properties in the resulting compounds. The strategic utilization of 5-Methylthiophene-2,3-dicarboxylic acid in chemical synthesis offers researchers a powerful tool for the efficient preparation of novel organic molecules with potential therapeutic applications.