37098-74-1 Usage
Uses
Used in Pharmaceutical Industry:
3-(Benzyloxy)piperidine is utilized as a key building block in organic synthesis for the preparation of a wide range of pharmaceuticals. Its unique structure and functional group contribute to the development of new drug molecules with improved therapeutic effects.
Used as Antipsychotic and Antidepressant Agent:
In the field of psychopharmacology, 3-(Benzyloxy)piperidine is employed as a potential antipsychotic and antidepressant agent. Its pharmacological properties have been studied for their ability to modulate neurotransmitter systems, offering new avenues for the treatment of mental health disorders.
Used in Neurodegenerative Disease Treatment:
3-(Benzyloxy)piperidine has been investigated for its potential application in the treatment of neurodegenerative diseases. Its biological activity suggests that it may have neuroprotective effects, offering hope for the development of new therapies to combat conditions such as Alzheimer's and Parkinson's diseases.
Used as Pain-Relief Medication:
In the realm of analgesics, 3-(Benzyloxy)piperidine has been explored for its potential as a pain-relief medication. Its pharmacological properties indicate that it may effectively target pain pathways, providing an alternative to existing pain management options.
Check Digit Verification of cas no
The CAS Registry Mumber 37098-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,9 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37098-74:
(7*3)+(6*7)+(5*0)+(4*9)+(3*8)+(2*7)+(1*4)=141
141 % 10 = 1
So 37098-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-2-5-11(6-3-1)10-14-12-7-4-8-13-9-12/h1-3,5-6,12-13H,4,7-10H2
37098-74-1Relevant articles and documents
B(C6F5)3-Catalyzed Cascade Reduction of Pyridines
Liu, Zhi-Yun,Wen, Zhi-Hui,Wang, Xiao-Chen
supporting information, p. 5817 - 5820 (2017/05/12)
B(C6F5)3 has been found to be an effective catalyst for reduction of pyridines and other electron-deficient N-heteroarenes with hydrosilanes (or hydroboranes) and amines as the reducing reagents. The success of this development hinges upon the realization of a cascade process of dearomative hydrosilylation (or hydroboration) and transfer hydrogenation. The broad functional-group tolerance (e.g. ketone, ester, unactivated olefins, nitro, nitrile, heterocycles, etc.) implies high practical utility.
Sulfamylbenzoic acids
-
, (2008/06/13)
Certain mono- and disubstituted-5-sulfamylbenzoic acids, many of which are novel, and their use in lowering blood lipid levels in mammals.