347389-75-7 Usage
Description
4,4,5,5-Tetramethyl-2-(1-propyn-1-yl)-1,3,2-dioxaborolane is a boron-containing chemical compound that belongs to the class of dioxaborolanes. It has a molecular formula of C9H15BO2 and a molecular weight of 164.02 g/mol. 4,4,5,5-Tetramethyl-2-(1-propyn-1-yl)-1,3,2-dioxaborolane is recognized for its versatility in organic synthesis and its ability to participate in various reactions, such as Suzuki-Miyaura cross-coupling.
Uses
Used in Organic Synthesis:
4,4,5,5-Tetramethyl-2-(1-propyn-1-yl)-1,3,2-dioxaborolane is used as a versatile reagent in organic synthesis for the preparation of a wide range of organic compounds. Its applications span across the development of pharmaceuticals, agrochemicals, and materials, making it a valuable component in these industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4,5,5-Tetramethyl-2-(1-propyn-1-yl)-1,3,2-dioxaborolane is utilized as a building block in the synthesis of complex organic molecules. Its ability to undergo Suzuki-Miyaura cross-coupling reactions allows for the creation of diverse pharmaceutical compounds, contributing to the advancement of drug discovery and development.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 4,4,5,5-Tetramethyl-2-(1-propyn-1-yl)-1,3,2-dioxaborolane serves as a key reagent in the synthesis of various agrochemicals. Its role in creating complex organic molecules aids in the production of effective and innovative products for agricultural applications.
Used in Materials Science:
In the field of materials science, 4,4,5,5-Tetramethyl-2-(1-propyn-1-yl)-1,3,2-dioxaborolane is employed for the synthesis of novel materials with specific properties. Its reactivity and ability to form cross-coupled products make it an important reagent in developing new materials with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 347389-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,7,3,8 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 347389-75:
(8*3)+(7*4)+(6*7)+(5*3)+(4*8)+(3*9)+(2*7)+(1*5)=187
187 % 10 = 7
So 347389-75-7 is a valid CAS Registry Number.
347389-75-7Relevant articles and documents
Development of a new building block for the synthesis of silicon-based drugs and odorants: Alternative synthesis of the retinoid agonist disila-bexarotene
Buettner, Matthias W.,Naetscher, Jennifer B.,Burschka, Christian,Tacke, Reinhold
, p. 4835 - 4838 (2007)
With 4,4,5,5-tetramethyl-2-(3,5,5,8,8-pentamethyl-5,8-disila-5,6,7,8- tetrahydro-2-naphthyl)-1,3,2-dioxaborolane (5) a new building block for the synthesis of biologically active 5,8-disila-5,6,7,8-tetrahydronaphthalene derivatives has been made available. The high synthetic potential of 5 has been demonstrated by the development of a new synthesis of the retinoid agonist disila-bexarotene (1).
Boron-directed regio- and stereoselective enyne cross metathesis: Efficient synthesis of vinyl boronate containing 1,3-dienes
Kim, Mansuk,Lee, Daesung
, p. 1865 - 1868 (2007/10/03)
(Chemical Equation Presented) Regio- and stereoselective enyne cross metathesis reactions between borylated alkynes and terminal alkenes were realized to provide a variety of functionalized vinyl boronates. High chemical yield and regioselectivity was ach
