94379-05-2 Usage
Description
(R,S)-N-benzylpiperidine-3-carboxamide, also known as (R,S)-BPC or AHN-086, is a chemical compound belonging to the piperidine class. It is a psychoactive drug with potential therapeutic applications in various neurological and psychiatric disorders.
Uses
Used in Pharmaceutical Industry:
(R,S)-N-benzylpiperidine-3-carboxamide is used as a potential treatment for neurological and psychiatric disorders due to its ability to modulate dopamine and serotonin levels in the brain. It is being studied for its potential as an antidepressant and antipsychotic medication.
Used in Neurological Disorders Treatment:
(R,S)-N-benzylpiperidine-3-carboxamide is used as a potential treatment for Parkinson's disease, as it may help in modulating the neurotransmitter levels affected by this condition.
Used in Psychiatric Disorders Treatment:
(R,S)-N-benzylpiperidine-3-carboxamide is used as a potential treatment for depression, given its effects on modulating neurotransmitter levels that are often imbalanced in individuals with this disorder.
Used in Addiction and Substance Abuse Treatment:
(R,S)-N-benzylpiperidine-3-carboxamide is used as a potential treatment for addiction and substance abuse, as it has been investigated for its potential to help individuals recover from these conditions.
However, it is important to note that further research is needed to fully understand the therapeutic potential and safety profile of (R,S)-N-benzylpiperidine-3-carboxamide.
Check Digit Verification of cas no
The CAS Registry Mumber 94379-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,7 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94379-05:
(7*9)+(6*4)+(5*3)+(4*7)+(3*9)+(2*0)+(1*5)=162
162 % 10 = 2
So 94379-05-2 is a valid CAS Registry Number.
94379-05-2Relevant articles and documents
Better than Nature: Nicotinamide Biomimetics That Outperform Natural Coenzymes
Knaus, Tanja,Paul, Caroline E.,Levy, Colin W.,De Vries, Simon,Mutti, Francesco G.,Hollmann, Frank,Scrutton, Nigel S.
supporting information, p. 1033 - 1039 (2016/02/05)
The search for affordable, green biocatalytic processes is a challenge for chemicals manufacture. Redox biotransformations are potentially attractive, but they rely on unstable and expensive nicotinamide coenzymes that have prevented their widespread expl
A convenient route to 1-benzyl 3-aminopyrrolidine and 3-aminopiperidine
Jean, Ludovic,Baglin, Isabelle,Rouden, Jacques,Maddaluno, Jacques,Lasne, Marie-Claire
, p. 5645 - 5649 (2007/10/03)
1-Benzyl 3-aminopyrrolidine 1 and 1-benzyl 3-aminopiperidine 2 were prepared rapidly mainly in aqueous conditions in 55 and 75% yields, respectively, on a multi-gram scale starting from inexpensive and commercially available starting materials. The key step involved the Curtius rearrangement mediated by sodium nitrite and trifluoroacetic acid of the appropriate acylhydrazides. All the reactions (except LAH reductions) were performed in water.
