1000303-67-2 Usage
Uses
Used in Pharmaceutical Industry:
4,5,6,7-tetrahydroisoxazolo[4,3-c]pyridine is used as a pharmaceutical intermediate for the development of new drugs due to its unique molecular structure and potential medicinal properties.
Used in Neuroprotective Applications:
In the field of neuroscience, 4,5,6,7-tetrahydroisoxazolo[4,3-c]pyridine is used as a neuroprotective agent, potentially offering protection to neurons and mitigating neuronal damage in various neurological disorders.
Used in Anti-inflammatory Applications:
4,5,6,7-tetrahydroisoxazolo[4,3-c]pyridine is utilized as an anti-inflammatory agent, suggesting its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Analgesic Applications:
As an analgesic, 4,5,6,7-tetrahydroisoxazolo[4,3-c]pyridine is employed for its pain-relieving properties, offering a potential therapeutic option for managing pain in various clinical settings.
Used in Neurotransmitter Receptor Modulation:
4,5,6,7-tetrahydroisoxazolo[4,3-c]pyridine is studied for its potential as a modulator of neurotransmitter receptors in the brain, making it a target for research in drug development for conditions related to neurotransmission dysregulation.
Check Digit Verification of cas no
The CAS Registry Mumber 1000303-67-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,3,0 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1000303-67:
(9*1)+(8*0)+(7*0)+(6*0)+(5*3)+(4*0)+(3*3)+(2*6)+(1*7)=52
52 % 10 = 2
So 1000303-67-2 is a valid CAS Registry Number.
1000303-67-2Relevant academic research and scientific papers
Nitrile oxide versus nitrone - Switching regioselectivity of intramolecular 1,3-dipolar cycloadditions towards the preparation of aminopiperidinecarboxylates
Wuerdemann, Martina,Christoffers, Jens
, p. 7421 - 7431 (2013/11/19)
3-(Allylamino)- and 3-(propargylamino)propanal were converted via the corresponding oximes into nitrile oxides, which readily underwent intramolecular 1,3-dipolar cycloadditions to furnish a piperidine-annulated isoxazole or isoxazoline. The annulated isoxazoline was transformed into orthogonally carbamate-protected cis- and trans-4-aminopiperidine-3-carboxylates, both representing interesting scaffolds for combinatorial chemistry. Through sequences of amidations and deprotections two triply functionalized products were obtained as examples for diversification. After Boc removal, the piperidino-annulated isoxazole was also subjected to diversifying reactions, such as reductive amination, amidation, and the formation of sulfonamido- and ureido-substituted derivatives. Intramolecular 1,3-dipolar cycloaddition of nitrile oxides is the key for the formation of aminopiperidines from acrolein and allylamines. Copyright
