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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)-

5-Tert-butoxycarbonylthiophene-2-boronic acid

OB(c1ccc(s1)C(=O)OC(C)(C)C)O Request for Quotation
Chemical Name: 5-Tert-butoxycarbonylthiophene-2-boronic acid
CAS Number: 925921-29-5
Product Number: AG00GYEL(AGN-PC-09TA1V)
Synonyms:
MDL No:
Molecular Formula: C9H13BO4S
Molecular Weight: 228.0731

Identification/Properties

Computed Properties
Molecular Weight:
228.069g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
228.063g/mol
Monoisotopic Mass:
228.063g/mol
Topological Polar Surface Area:
95A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
239
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (5-(tert-Butoxycarbonyl)thiophen-2-yl)boronic acid, commonly known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely utilized in the field of organic chemistry for its exceptional reactivity and compatibility with various functional groups. $name$ is commonly employed in Suzuki-Miyaura cross-coupling reactions, a fundamental transformation in organic synthesis that allows for the formation of carbon-carbon bonds under mild conditions. Its boronic acid group readily participates in this reaction, facilitating the synthesis of biaryl compounds, which are prevalent in pharmaceuticals, agrochemicals, and materials science.Additionally, $name$ can serve as a key intermediate in the synthesis of complex molecules such as pharmaceuticals, natural products, and materials. Its unique structure and properties make it a valuable tool for chemists seeking to design and create novel compounds with specific functionalities.Overall, the application of (5-(tert-Butoxycarbonyl)thiophen-2-yl)boronic acid in chemical synthesis extends far beyond simple coupling reactions, offering researchers a powerful tool for accessing diverse chemical space and driving innovation in the field of organic chemistry.