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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-bromo-5-chlorothiophen-2-yl)boronic acid

OB(c1cc(c(s1)Cl)Br)O Request for Quotation
Chemical Name: (4-bromo-5-chlorothiophen-2-yl)boronic acid
CAS Number: 1150114-72-9
Product Number: AG000FN7(AGN-PC-07XUEQ)
Synonyms:
MDL No:
Molecular Formula: C4H3BBrClO2S
Molecular Weight: 241.2984

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
241.29g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
239.882g/mol
Monoisotopic Mass:
239.882g/mol
Topological Polar Surface Area:
68.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
128
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


The (4-Bromo-5-chlorothiophen-2-yl)boronic acid is a versatile chemical reagent commonly used in organic synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. Through its boronic acid functionality, it readily participates in Suzuki coupling reactions with aryl halides or pseudohalides, enabling the efficient formation of carbon-carbon bonds. This makes it a crucial tool for the construction of complex molecular structures in medicinal chemistry and materials science. Additionally, (4-Bromo-5-chlorothiophen-2-yl)boronic acid is employed in the synthesis of heterocyclic compounds, where its unique structure imparts desirable properties and functionalities. Its strategic incorporation into organic molecules allows for the modulation of biological activity, making it a valuable reagent in drug discovery and development. Furthermore, this compound finds application in the preparation of organic electronic materials, where its conjugated system contributes to the desired electronic properties. The utilization of (4-Bromo-5-chlorothiophen-2-yl)boronic acid in chemical synthesis showcases its significance in advancing various scientific fields and underscores its importance as a key tool for molecular design and innovation.