65210-99-3 Usage
Description
(2-Benzenesulfonyl-2-bromo-ethyl)-cyclohexyl-amine is a sulfonylamine organic compound characterized by a benzenesulfonyl group attached to a 2-bromo-ethyl group, which is further connected to a cyclohexyl-amine group. It is utilized in organic synthesis and medicinal chemistry for the creation of biologically active molecules and pharmaceutical drug development.
Uses
Used in Organic Synthesis:
(2-Benzenesulfonyl-2-bromo-ethyl)-cyclohexyl-amine serves as a key building block in organic synthesis, contributing to the formation of various complex organic molecules with potential applications in different fields.
Used in Medicinal Chemistry:
In the realm of medicinal chemistry, (2-Benzenesulfonyl-2-bromo-ethyl)-cyclohexyl-amine is employed for the synthesis of biologically active molecules, which may possess therapeutic properties and contribute to the development of new pharmaceutical drugs.
Used in Pharmaceutical Drug Development:
(2-BENZENESULFONYL-2-BROMO-ETHYL)-CYCLOHEXYL-AMINE plays a significant role in the development of pharmaceutical drugs, potentially leading to the discovery of novel treatments and medications for various medical conditions.
Used in Research and Industry:
(2-Benzenesulfonyl-2-bromo-ethyl)-cyclohexyl-amine may also have other potential applications in research and industry, where its unique structure and properties can be explored for innovative uses and advancements.
Check Digit Verification of cas no
The CAS Registry Mumber 65210-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,1 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65210-99:
(7*6)+(6*5)+(5*2)+(4*1)+(3*0)+(2*9)+(1*9)=113
113 % 10 = 3
So 65210-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H20BrNO2S/c15-14(11-16-12-7-3-1-4-8-12)19(17,18)13-9-5-2-6-10-13/h2,5-6,9-10,12,14,16H,1,3-4,7-8,11H2
65210-99-3Relevant articles and documents
Improved heteroatom nucleophilic addition to electron-poor alkenes promoted by CeCl3·7H2O/NaI system supported on alumina in solvent-free conditions
Bartoli, Giuseppe,Bartolacci, Massimo,Giuliani, Arianna,Marcantoni, Enrico,Massaccesi, Massimo,Torregiani, Elisabetta
, p. 169 - 174 (2007/10/03)
(Chemical Equation Presented). Conjugate addition of heteroatom nucleophiles to carbon-carbon double bonds conjugated with a strong electron-withdrawing group is one of the most important new bond-forming strategies in synthetic organic chemistry. Among the methods for these Michael additions, Lewis acids have shown the best promoter activity, and in particular, the use of reagents impregnated over inorganic supports is rapidly increased. With the increase of environmental consciousness in chemical research, the solvent-free Michael addition has attracted our attention. In continuation of our ongoing program to develop synthetic protocols utilizing cerium trichloride, we report an extension of the CeCl3·7H2O/NaI combination supported under solvent-free conditions to promote heteroatom Michael addition. Using neutral alumina (Al2O3) as solid support permits us to circumvent some of the problems associated with the procedure where the inorganic support is silica gel. The CeCl 3· 7H2O/NaI/Al2O3 system works well for hetero-Michael additions utilizing weakly nucleophiles such as imidazoles and carbamates, and also the reaction proceeds with good yields in the case of Michael acceptors different from α,β-unsaturated carbonyl compounds. An important synthetic application of this our methodology is the intramolecular aza-Michael reaction in producing 4-piperidinone derivatives, which are of interest as synthetic intermediates toward important classes of heterocycles.
