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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)-

Boronic acid, (4-acetyl-2-thienyl)-

OB(c1scc(c1)C(=O)C)O Request for Quotation
Chemical Name: Boronic acid, (4-acetyl-2-thienyl)-
CAS Number: 689247-77-6
Product Number: AG0060G0(AGN-PC-07AD50)
Synonyms:
MDL No:
Molecular Formula: C6H7BO3S
Molecular Weight: 169.9940

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
169.989g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
170.021g/mol
Monoisotopic Mass:
170.021g/mol
Topological Polar Surface Area:
85.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
162
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


The (4-Acetylthiophen-2-yl)boronic acid is a versatile compound widely used in chemical synthesis as a key building block in the formation of new organic molecules. When incorporated into various reaction schemes, this specific boronic acid derivative serves as a crucial substrate for Suzuki-Miyaura cross-coupling reactions. Through these reactions, (4-Acetylthiophen-2-yl)boronic acid can be combined with various aryl or vinyl halides under the catalysis of palladium to form biaryl or vinylic compounds. This process enables the synthesis of complex organic molecules with diverse applications in the pharmaceutical, agrochemical, and materials science industries. Additionally, the (4-Acetylthiophen-2-yl)boronic acid plays a vital role in the development of novel drug candidates, advanced materials, and functionalized organic compounds through its participation in cross-coupling and other organic transformations.