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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, 4-(4-methoxyphenyl)-

COc1ccc(cc1)c1csc(c1)C(=O)O Request for Quotation
Chemical Name: 2-Thiophenecarboxylic acid, 4-(4-methoxyphenyl)-
CAS Number: 82437-74-9
Product Number: AG008JZ4(AGN-PC-0KK823)
Synonyms:
MDL No:
Molecular Formula: C12H10O3S
Molecular Weight: 234.2710

Identification/Properties

Computed Properties
Molecular Weight:
234.269g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
234.035g/mol
Monoisotopic Mass:
234.035g/mol
Topological Polar Surface Area:
74.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
249
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:
H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(4-Methoxyphenyl)thiophene-2-carboxylic acid, commonly known as $name$, plays a pivotal role in organic chemical synthesis as a versatile building block. This compound is widely utilized in the pharmaceutical industry for the development of pharmaceutical drugs and drug intermediates. Its unique structure and reactive properties make it a valuable precursor in the synthesis of various biologically active compounds.In chemical synthesis, $name$ serves as a key starting material for the preparation of diversified heterocyclic compounds. Its functional groups enable facile derivatization, allowing for the introduction of different substituents to modulate the properties of the final products. By incorporating 4-(4-Methoxyphenyl)thiophene-2-carboxylic acid into organic synthesis routes, chemists can access a wide range of novel molecules with potential applications in medicinal chemistry and material science.Moreover, the presence of a thiophene ring in the structure of 4-(4-Methoxyphenyl)thiophene-2-carboxylic acid imparts desirable electronic properties to the synthesized compounds. This feature makes it particularly valuable in the design and synthesis of organic semiconductors, light-emitting materials, and other electronic components.Overall, 4-(4-Methoxyphenyl)thiophene-2-carboxylic acid is an indispensable tool in the hands of synthetic chemists, enabling the creation of diverse molecules with tailored functionalities and applications in various fields of chemistry and beyond.