280-97-7 Usage
Description
9-AZABICYCLO[3,3,1]NONANE is a chemical compound belonging to the class of azabicycloalkanes, which are nitrogen-containing bicyclic hydrocarbons. It is characterized by its unique molecular structure, featuring a nine-membered ring with one nitrogen atom and eight carbon atoms. 9-AZABICYCLO[3,3,1]NONANE is known for its potential applications in various chemical and pharmaceutical processes due to its distinct properties.
Uses
Used in Chemical Synthesis:
9-AZABICYCLO[3,3,1]NONANE is used as a reactant in the preparation of azabicyclo[3.3.1]nonane N-oxyl, which is an important intermediate in the synthesis of various organic compounds. 9-AZABICYCLO[3,3,1]NONANE serves as a key building block for the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 9-AZABICYCLO[3,3,1]NONANE may be used as a starting material or intermediate for the synthesis of various drug candidates. Its unique structure and properties make it a valuable component in the development of novel therapeutic agents, particularly those targeting complex biological systems.
Used in Material Science:
9-AZABICYCLO[3,3,1]NONANE could also find applications in the field of material science, where it may be utilized in the development of new materials with specific properties. Its unique molecular structure could contribute to the creation of advanced materials with potential uses in various industries, such as electronics, aerospace, or automotive.
Check Digit Verification of cas no
The CAS Registry Mumber 280-97-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 280-97:
(5*2)+(4*8)+(3*0)+(2*9)+(1*7)=67
67 % 10 = 7
So 280-97-7 is a valid CAS Registry Number.
280-97-7Relevant articles and documents
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Nelsen,Kessel
, p. 2503 (1979)
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Preparation of ABNO on Scale and Analysis by Quantitative Paramagnetic NMR
Song, Zhiguo J.,Zhou, Guoyue,Cohen, Ryan,Tan, Lushi
, p. 1257 - 1261 (2018/09/06)
A practical, safe, and scalable synthesis of the stable nitro-oxide radical catalyst ABNO was developed. This process is chromatography-free and avoids the Wolff-Kishner reduction. 1H NMR data for this paramagnetic compound were obtained that allowed an assessment of its chemical purity. Impact sensitivity test data for solid ABNO are also reported.
An expeditious entry to 9-azabicyclo[3.3.1]nonane N-oxyl (ABNO): Another highly active organocatalyst for oxidation of alcohols
Shibuya, Masatoshi,Tomizawa, Masaki,Sasano, Yusuke,Iwabuchi, Yoshiharu
supporting information; experimental part, p. 4619 - 4622 (2009/09/08)
(Chemical Equation Presented) A practical, three-step synthetic route to 9-azabicyclo[3.3.1] nonane N-oxyl (ABNO, 3), an unhindered, stable class of nitroxyl radical, has been developed. ABNO exhibits a highly active nature compared with TEMPO in the catalytic oxidation of alcohols to their corresponding carbonyl compounds.
