462636-88-0 Usage
Description
4,4,5,5-Tetramethyl-2-(2-phenyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane is a complex organic compound characterized by its unique molecular structure, which includes a dioxaborolane ring fused to a cyclohexenyl group and a phenyl group. 4,4,5,5-TETRAMETHYL-2-(2-PHENYL-1-CYCLOHEXEN-1-YL)-1,3,2-DIOXABOROLANE is known for its reactivity and stability, making it a valuable intermediate in organic synthesis.
Uses
Used in Pharmaceutical Industry:
4,4,5,5-Tetramethyl-2-(2-phenyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane is used as a reactant in the stereoselective preparation of cyclic boronate derivatives. This application is crucial for the synthesis of pharmaceutical compounds, as it allows for the creation of specific stereoisomers that can have different biological activities and properties.
Used in Chemical Research:
In the field of chemical research, 4,4,5,5-Tetramethyl-2-(2-phenyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane serves as a versatile building block for the development of new organic compounds. Its unique structure and reactivity make it an attractive candidate for exploring novel reactions and mechanisms, potentially leading to the discovery of new chemical processes and products.
Used in Material Science:
4,4,5,5-Tetramethyl-2-(2-phenyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane can also be utilized in material science for the development of advanced materials with specific properties. Its incorporation into polymers or other materials could lead to new applications in areas such as electronics, coatings, or adhesives, where its unique structure and reactivity may provide advantages over existing materials.
Overall, 4,4,5,5-Tetramethyl-2-(2-phenyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane is a versatile and valuable compound with applications across various industries, including pharmaceuticals, chemical research, and material science. Its unique structure and reactivity make it an important tool for the synthesis of new compounds and the development of innovative materials and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 462636-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,2,6,3 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 462636-88:
(8*4)+(7*6)+(6*2)+(5*6)+(4*3)+(3*6)+(2*8)+(1*8)=170
170 % 10 = 0
So 462636-88-0 is a valid CAS Registry Number.
462636-88-0Relevant articles and documents
Oxidation of Nonactivated Anilines to Generate N-Aryl Nitrenoids
Deng, Tianning,Mazumdar, Wrickban,Ford, Russell L.,Jana, Navendu,Izar, Ragda,Wink, Donald J.,Driver, Tom G.
supporting information, p. 4456 - 4463 (2020/03/05)
A low-temperature, protecting-group-free oxidation of 2-substituted anilines has been developed to generate an electrophilic N-aryl nitrenoid intermediate that can engage in C-NAr bond formation to construct functionalized N-heterocycles. The exposure of 2-substituted anilines to PIFA and trifluoroacetic acid or 10 mol percent Sc(OTf)3 triggers nitrenoid formation, followed by productive and selective C-NAr and C-C bond formation to yield spirocyclic- or bicyclic 3H-indoles or benzazepinones. Our experiments demonstrate the breadth of these oxidative processes, uncover underlying fundamental elements that control selectivity, and demonstrate how the distinct reactivity patterns embedded in N-aryl nitrenoid reactive intermediates can enable access to functionalized 3H-indoles or benzazepinones.
Preparation of alkylmagnesium reagents from alkenes through hydroboration and boron-magnesium exchange
Reichle, Markus A.,Breit, Bernhard
supporting information; experimental part, p. 5730 - 5734 (2012/08/14)
Tolerant: Alkylmagnesium reagents can be synthesized from alkenes through a sequence of hydroboration and subsequent boron-magnesium exchange using a method that tolerates different functional groups (see scheme). The resulting alkylmagnesium reagents can be used in carbon-carbon bond forming reactions, such as alkylation reactions or transition-metal-catalyzed cross-coupling reactions. Copyright
