57727-91-0 Usage
Description
(1S)-8-benzyl-3-methyl-3,8-diazabicyclo[3.2.1]octane is a bicyclic, nitrogen-containing chiral compound with a single stereocenter at the first carbon atom. It features a benzyl group and a methyl group attached to the nitrogen atoms, which contribute to its unique chemical properties and potential applications.
Uses
Used in Asymmetric Catalysis:
(1S)-8-benzyl-3-methyl-3,8-diazabicyclo[3.2.1]octane is used as a ligand in asymmetric catalysis for its ability to induce selectivity in chemical reactions, leading to the preferential formation of one enantiomer over another. This is crucial in the synthesis of chiral molecules, which often have different biological activities and are important in pharmaceuticals and agrochemicals.
Used in Organic Synthesis:
In the field of organic synthesis, (1S)-8-benzyl-3-methyl-3,8-diazabicyclo[3.2.1]octane serves as a versatile building block and catalyst. Its unique structure allows it to participate in various organic reactions, facilitating the formation of complex molecules and enhancing the efficiency of synthetic processes.
Used in Pharmaceutical Research:
(1S)-8-benzyl-3-methyl-3,8-diazabicyclo[3.2.1]octane is also studied for its potential pharmacological properties. Its ability to interact with neurotransmitter receptors in the central nervous system suggests that it may have applications in the development of drugs targeting neurological disorders or conditions related to neurotransmission.
Used in Chemical Biology:
Due to its interaction with biological targets, (1S)-8-benzyl-3-methyl-3,8-diazabicyclo[3.2.1]octane can be utilized in chemical biology for probing and understanding the mechanisms of biological systems. It may serve as a tool compound to investigate receptor binding, signal transduction pathways, and other cellular processes.
Check Digit Verification of cas no
The CAS Registry Mumber 57727-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,2 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57727-91:
(7*5)+(6*7)+(5*7)+(4*2)+(3*7)+(2*9)+(1*1)=160
160 % 10 = 0
So 57727-91-0 is a valid CAS Registry Number.
57727-91-0Relevant articles and documents
CYCLOPROPYL FUSED INDOLOBENZAZEPINE HCV NS5B INHIBITORS
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Page/Page column 67-68, (2009/06/27)
The invention encompasses compounds of formula (I) as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV
Diazabicyclooctanes and diazabicycloheptanes
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, (2008/06/13)
Twelve analogs of diethylcarbamazine as prepared by acylation of 3- and 8-methyl-3,8-diazabicyclo[3.2.1]octane, 2-methyl-2,5-diazabicyclo[2.2.2]octane, and 2-methyl-2,5-diazabicyclo [2.2.1]heptane with diethylcarbamyl chloride, ethyl chloroformate, ethyl isocyanate, and cyclohexanecarbonyl chloride. These compounds are formally derived from diethylcarbamazine in possessing two- or one-carbon bridges over the piperazine ring. The compounds have utility as antifilarial agents and as bronchodilators.
