1198604-53-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Benzyl-3-azabicyclo[3.1.0]hexan-2-one serves as a crucial intermediate in the synthesis of various pharmaceuticals due to its ability to be incorporated into the molecular structures of drugs with desired therapeutic effects. Its presence in drug molecules can contribute to their analgesic, anticonvulsant, and anti-inflammatory properties, making it instrumental in the development of medications for pain management, seizure control, and inflammation reduction.
Used in Drug Discovery and Development:
In the realm of drug discovery and development, 3-Benzyl-3-azabicyclo[3.1.0]hexan-2-one is utilized as a key component in the design and synthesis of new molecules with potential therapeutic applications. Its unique structure allows for the exploration of novel chemical entities that could address unmet medical needs, offering a valuable asset in the advancement of pharmaceutical research.
Used in Biological Research:
3-Benzyl-3-azabicyclo[3.1.0]hexan-2-one is also employed in biological research to study its pharmacological activities and to understand its mechanisms of action. This research can provide insights into the compound's potential as a therapeutic agent and inform the development of new drugs with improved efficacy and safety profiles.
Handling and Synthesis:
Due to the complex nature of 3-Benzyl-3-azabicyclo[3.1.0]hexan-2-one, its handling and synthesis often require specialized equipment and expertise in organic chemistry. This ensures that the compound is produced and manipulated safely and effectively, facilitating its use in various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1198604-53-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,6,0 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1198604-53:
(9*1)+(8*1)+(7*9)+(6*8)+(5*6)+(4*0)+(3*4)+(2*5)+(1*3)=183
183 % 10 = 3
So 1198604-53-3 is a valid CAS Registry Number.
1198604-53-3Relevant academic research and scientific papers
Olefin cyclopropanations via sequential atom transfer radical addition-dechlorination reactions
Thommes, Katrin,Severin, Kay
experimental part, p. 188 - 190 (2011/07/07)
In organic synthesis, cyclopropanation reactions are often performed with Simmons-Smith-type reagents or by transition metal catalyzed reactions of olefins with diazo compounds. A novel method for the synthesis of substituted cyclopropanes is described that is based on a two-step reaction sequence. Olefins are reacted with 1,1'-dichlorides in a Ru-catalyzed atom transfer radical addition (ATRA) process and the resulting 1,3-dichlorides are directly converted into cyclopropanes by reductive coupling with magnesium. This one-pot procedure is applicable to a variety of substrates and can be performed in an inter- or intramolecular fashion. Schweizerische Chemische Gesellschaft.
Olefin cyclopropanation by a sequential atom-transfer radical addition and dechlorination in the presence of a ruthenium catalyst
Thommes, Katrin,Kiefer, Gregor,Scopelliti, Rosario,Severin, Kay
supporting information; experimental part, p. 8115 - 8119 (2010/01/16)
Without diazo: The reductive coupling of olefins with dichloro compounds in the presence of a ruthenium catalyst and magnesium gives cyclopropanes in good yield (see scheme).
