664991-83-7 Usage
Uses
Used in Organic Synthesis:
4,4,5,5-Tetramethyl-2-(4-(oxiran-2-ylmethoxy)phenyl)-1,3,2-dioxaborolane is used as a reagent in organic synthesis for its ability to form carbon-carbon bonds through the Suzuki-Miyaura coupling reaction. This reaction is a powerful tool in the construction of complex organic molecules, making 4,4,5,5-TETRAMETHYL-2-(4-(OXIRAN-2-YLMETHOXY)PHENYL)-1,3,2-DIOXABOROLANE an essential component in the synthesis process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4,5,5-Tetramethyl-2-(4-(oxiran-2-ylmethoxy)phenyl)-1,3,2-dioxaborolane is used as a key intermediate in the synthesis of potential drug candidates. Its reactivity and stability make it a valuable building block for the development of new and innovative pharmaceutical compounds.
Used in Agrochemical Industry:
4,4,5,5-Tetramethyl-2-(4-(oxiran-2-ylmethoxy)phenyl)-1,3,2-dioxaborolane is also utilized in the agrochemical industry for the development of new pesticides and herbicides. Its ability to form carbon-carbon bonds and its stability make it a valuable component in the creation of effective and environmentally friendly agrochemicals.
Used in Materials Science:
In materials science, 4,4,5,5-Tetramethyl-2-(4-(oxiran-2-ylmethoxy)phenyl)-1,3,2-dioxaborolane has potential applications in the development of novel materials and polymers. Its unique chemical properties and reactivity make it a promising candidate for the synthesis of advanced materials with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 664991-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,4,9,9 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 664991-83:
(8*6)+(7*6)+(6*4)+(5*9)+(4*9)+(3*1)+(2*8)+(1*3)=217
217 % 10 = 7
So 664991-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H21BO4/c1-14(2)15(3,4)20-16(19-14)11-5-7-12(8-6-11)17-9-13-10-18-13/h5-8,13H,9-10H2,1-4H3
664991-83-7Relevant articles and documents
Switchable Chemoselectivity of Reactive Intermediates Formation and Their Direct Use in A Flow Microreactor
Ashikari, Yosuke,Tamaki, Takashi,Kawaguchi, Tomoko,Furusawa, Mai,Yonekura, Yuya,Ishikawa, Susumu,Takahashi, Yusuke,Aizawa, Yoko,Nagaki, Aiichiro
supporting information, p. 16107 - 16111 (2021/10/12)
A chemoselectivity switchable microflow reaction was developed to generate reactive and unstable intermediates. The switchable chemoselectivity of this reaction enables a selection for one of two different intermediates, an aryllithium or a benzyl lithium, at will from the same starting material. Starting from bromo-substituted styrenes, the aryllithium intermediates were converted to the substituted styrenes, whereas the benzyl lithium intermediates were engaged in an anionic polymerization. These chemoselectivity-switchable reactions can be integrated to produce polymers that cannot be formed during typical polymerization reactions.
SUBSTITUTED PYRROLOPYRIDINES
-
Page 55, (2010/11/30)
There are provided novel compounds of formula (I) wherein R1, R2 and R3 are as defined in the specification and pharmaceutically acceptable salts thereof; together with processes for their preparation, compositions containing them and their use in therapy. The compounds are inhibitors of the kinase Itk.
