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2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a chemical compound characterized by the presence of a boron atom. It is renowned for its high stability, low toxicity, and versatility in a broad spectrum of organic reactions. 2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane's unique structure and reactivity render it an indispensable tool in medicinal chemistry and materials science, particularly for the synthesis of complex organic molecules and the development of functional materials.

1256359-13-3

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1256359-13-3 Usage

Uses

Used in Organic Synthesis:
2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a crucial reagent in organic synthesis, facilitating the formation of carbon-carbon bonds through the Suzuki coupling reaction. This reaction is highly valued for its ability to join aryl and vinyl halides to arylboronic acids or esters, thereby expanding the scope of synthetic organic chemistry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is utilized for the creation of complex organic molecules with potential therapeutic applications. Its reactivity and stability contribute to the development of novel pharmaceutical agents, enhancing drug discovery and design processes.
Used in Materials Science:
2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane also finds application in materials science, where it is employed in the synthesis of functional materials with specific properties. These materials can be tailored for various applications, such as in electronics, energy storage, or as components of advanced materials with unique characteristics.
Used in the Suzuki Coupling Reaction:
2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a reagent in the Suzuki coupling reaction for the formation of carbon-carbon bonds. This reaction is particularly useful in the synthesis of biologically active compounds and the construction of molecular frameworks with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials development.

Check Digit Verification of cas no

The CAS Registry Mumber 1256359-13-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1256359-13:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*9)+(2*1)+(1*3)=163
163 % 10 = 3
So 1256359-13-3 is a valid CAS Registry Number.

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