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  2. 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid

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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)-

4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid

OC(=O)c1scc(c1)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid
CAS Number: 1010836-19-7
Product Number: AG0003P5(AGN-PC-00YV2V)
Synonyms:
MDL No:
Molecular Formula: C11H15BO4S
Molecular Weight: 254.1104

Identification/Properties

Computed Properties
Molecular Weight:
254.107g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
254.078g/mol
Monoisotopic Mass:
254.078g/mol
Topological Polar Surface Area:
84A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
315
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique structure and reactivity. This compound is commonly employed in organic synthesis for the introduction of the thiophene moiety into complex molecular frameworks. The boronic acid functionality enables facile cross-coupling reactions, such as Suzuki-Miyaura coupling, allowing for the efficient formation of carbon-carbon bonds.Additionally, the presence of the carboxylic acid group offers opportunities for further derivatization through amidation, esterification, or other functional group transformations. The resulting derivatives of $name$ can exhibit varied properties and functionalities, making them valuable intermediates in the preparation of pharmaceuticals, agrochemicals, and advanced materials. In summary, the strategic incorporation of 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid in chemical synthesis enables the synthesis of diverse, structurally complex molecules with potential applications in various fields of research and industry.