1256359-02-0 Usage
Uses
Used in Organic Synthesis:
2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a reagent for the introduction of the boronic acid functionality into organic molecules, facilitating the synthesis of various organic compounds.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a key intermediate in the development of new drugs, owing to its ability to form stable boron-containing compounds with potential therapeutic properties.
Used in Material Science:
2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is employed as a precursor in the synthesis of advanced materials with unique properties, such as boron-containing polymers and nanomaterials, for various applications in material science.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the production of fine chemicals and pharmaceuticals, 2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a coupling partner in Suzuki-Miyaura cross-coupling reactions, a widely used method for the formation of carbon-carbon bonds, enabling the synthesis of complex molecular structures with high selectivity and efficiency.
Check Digit Verification of cas no
The CAS Registry Mumber 1256359-02-0 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, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1256359-02:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*9)+(2*0)+(1*2)=160
160 % 10 = 0
So 1256359-02-0 is a valid CAS Registry Number.