937591-32-7 Usage
Description
1-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-1-yl)ethanone is a complex chemical compound featuring an indoline ring and a boron-containing dioxaborolane group. As an ethanone derivative, it possesses a ketone functional group with an ethyl side chain. 1-(5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)INDOLIN-1-YL)ETHANONE holds potential in organic synthesis and pharmaceutical research due to its unique structure and reactivity. The presence of the boron-containing group also indicates its utility as a reagent in organic and inorganic chemistry, particularly in the formation of C-B bonds. The complex structure and potential reactivity of 1-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-1-yl)ethanone make it an intriguing compound for further study and potential applications.
Uses
Used in Organic Synthesis:
1-(5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)INDOLIN-1-YL)ETHANONE is used as a key intermediate for the synthesis of various organic compounds. Its unique structure and reactivity allow for the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)INDOLIN-1-YL)ETHANONE is used as a starting material for the development of new drugs. Its complex structure and potential reactivity make it a valuable compound for designing and synthesizing novel pharmaceutical agents.
Used in Organic and Inorganic Chemistry:
1-(5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)INDOLIN-1-YL)ETHANONE is used as a reagent in the formation of C-B bonds, which are essential in the synthesis of various organic and inorganic compounds. Its boron-containing group provides a unique platform for further chemical modifications and reactions.
Overall, 1-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-1-yl)ethanone is a versatile compound with potential applications in various fields, including organic synthesis, pharmaceutical research, and organic and inorganic chemistry. Its unique structure and reactivity make it a promising candidate for further study and development.
Check Digit Verification of cas no
The CAS Registry Mumber 937591-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,5,9 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 937591-32:
(8*9)+(7*3)+(6*7)+(5*5)+(4*9)+(3*1)+(2*3)+(1*2)=207
207 % 10 = 7
So 937591-32-7 is a valid CAS Registry Number.
937591-32-7Relevant articles and documents
Nickel-Catalyzed Borylation of Aryl- and Benzyltrimethylammonium Salts via C-N Bond Cleavage
Hu, Jiefeng,Sun, Heqing,Cai, Wangshui,Pu, Xinghui,Zhang, Yemin,Shi, Zhuangzhi
, p. 14 - 24 (2016/01/15)
By developing a mild Ni-catalyzed system, a method for direct borylation of sp2 and sp3 C-N bonds has been established. The key to this hightly efficient C-N bond borylative cleavage depends on the appropriate choice of the nickel catalyst Ni(COD)2, ICy·HCl as a ligand, and the use of 2-ethoxyethanol as the cosolvent. This transformation shows good functional group compatibility and can serve as a powerful synthetic tool for gram-scale synthesis and late-stage C-N borylation of complex compounds.
NEW COMPOUNDS
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Page/Page column 81, (2008/06/13)
This invention relates to novel compounds having the structural formula I below: and to their pharmaceutically acceptable salt, compositions and methods of use. These novel compounds provide a treatment or prophylaxis of cognitive impairment, Alzheimer Disease, neurodegeneration and dementia.
