cas 36155-74-5|| where to buy (2-Acetylthiophen-3-yl)boronic acid

Nombre del producto:(2-Acetylthiophen-3-yl)boronic acid

IUPAC Name:(2-acetylthiophen-3-yl)boronic acid

: CAS：36155-74-5; Fórmula molecular：C6H7BO3S; Pureza：95%

: Número de catálogo：CM134437; Peso molecular：169.99

Unidad de embalaje	Stock disponible	Precio($)
CM134437-1g	in stock	ȯȯ
CM134437-5g	in stock	ȅǑȅ

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Detalles del producto

: Núm. De CAS :36155-74-5; Fórmula molecular:C6H7BO3S; Punto de fusión:-; Código de sonrisas:O=C(C1=C(B(O)O)C=CS1)C; Densidad:

: Número de catálogo:CM134437; Peso molecular:169.99; Punto de ebullición:; Nº Mdl:MFCD01318932; Almacenamiento:

Category Infos

: Thiophenes; Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.

: Boronic Acids and Esters; Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).; Boronic Acid For Sale; Find trusted boronic acid for sale. Any requirements and problems can ask us at any time.

Column Infos

: Boronic Acids and Esters

Product Other Information

Product Overview	(2-Acetylthiophen-3-yl)boronic acid, commonly referred to as ATB, is an organic compound with a variety of applications in scientific research. It is a boronic acid derivative that is used in synthetic organic chemistry as a reagent for the synthesis of compounds, as well as in biochemistry and pharmacology to study the structure and function of proteins and other biomolecules.
Synthesis and Application	ATB can be synthesized by several different methods. One method involves the condensation of 2-acetylthiophene with boronic acid in aqueous acetic acid. The reaction is typically conducted at room temperature and yields a white solid product. Other methods include the reaction of 2-acetylthiophene with boronic acid in the presence of a base, such as sodium hydroxide, or the reaction of 2-acetylthiophene with boronic acid in the presence of a catalyst, such as pyridine. ATB has a variety of applications in scientific research. It has been used in in vivo and in vitro studies to study the structure and function of proteins and other biomolecules. It has also been used in the synthesis of compounds, as a reagent for the synthesis of pharmaceuticals, and in the development of biosensors.
Future Directions	There are a variety of potential future directions for research on ATB. These include further studies on its mechanism of action, biological activity, biochemical and physiological effects, and pharmacodynamics. Additionally, further studies could be conducted on its use in the synthesis of compounds, its use as a reagent for the synthesis of pharmaceuticals, and its use in the development of biosensors. Furthermore, further studies could be conducted on its use in in vivo and in vitro studies to study the structure and function of proteins and other biomolecules. Finally, further studies could be conducted on its advantages and limitations for lab experiments.