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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, 5-phenyl-

OC(=O)c1ccc(s1)c1ccccc1 Request for Quotation
Chemical Name: 2-Thiophenecarboxylic acid, 5-phenyl-
CAS Number: 19163-24-7
Product Number: AG002FDV(AGN-PC-0JVOE9)
Synonyms:
MDL No: MFCD01313432
Molecular Formula: C11H8O2S
Molecular Weight: 204.2450

Identification/Properties

Properties
MP:
186-190°C
BP:
393.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
204.243g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
204.025g/mol
Monoisotopic Mass:
204.025g/mol
Topological Polar Surface Area:
65.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Phenylthiophene-2-carboxylic acid is a valuable building block in chemical synthesis, particularly in the field of organic chemistry. This compound plays a crucial role in the creation of various organic molecules and pharmaceuticals due to its versatile nature and reactive properties.One key application of 5-Phenylthiophene-2-carboxylic acid is its use as a precursor in the synthesis of heterocyclic compounds. By incorporating this compound into chemical reactions, chemists can access a diverse range of heterocycles with unique structural properties and potential biological activities. Additionally, the presence of both a phenyl group and a carboxylic acid moiety in the molecule provides multiple sites for functionalization, allowing for further chemical modifications and customization of the final product.Moreover, 5-Phenylthiophene-2-carboxylic acid can serve as a starting material for the synthesis of advanced materials such as polymers, liquid crystals, and electronic components. Its ability to participate in various coupling reactions and transformations makes it a versatile intermediate in the preparation of complex organic materials with tailored properties and functionalities.Overall, the strategic use of 5-Phenylthiophene-2-carboxylic acid in chemical synthesis enables chemists to access a diverse array of molecules with applications spanning medicinal chemistry, material science, and other interdisciplinary fields.