17087-50-2 Usage
Uses
Used in Pharmaceutical Industry:
Benzenemethanamine, 2-methoxy-a-methyl-, hydrochloride is used as an analgesic agent for the management of moderate to severe pain. Its efficacy in pain relief is attributed to its action as a serotonin-norepinephrine reuptake inhibitor and a mu-opioid receptor agonist, which helps in alleviating discomfort and improving the quality of life for patients suffering from various painful conditions.
Used in Research and Development:
In the scientific community, Benzenemethanamine, 2-methoxy-a-methyl-, hydrochloride serves as a subject for research and development. Its psychoactive properties and potential for abuse make it a crucial compound for studying the mechanisms of addiction and the development of new treatments or interventions to combat substance misuse and dependence.
Used in Regulatory and Forensic Analysis:
Due to its classification as a controlled substance and its potential for misuse, Benzenemethanamine, 2-methoxy-a-methyl-, hydrochloride is utilized in regulatory and forensic analysis. It is an essential component in the identification and monitoring of illicit drug use, as well as in the development of policies and strategies to control and prevent the abuse of this potent opioid medication.
Check Digit Verification of cas no
The CAS Registry Mumber 17087-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,8 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17087-50:
(7*1)+(6*7)+(5*0)+(4*8)+(3*7)+(2*5)+(1*0)=112
112 % 10 = 2
So 17087-50-2 is a valid CAS Registry Number.
17087-50-2Relevant academic research and scientific papers
Sequential reductive amination-hydrogenolysis: A one-pot synthesis of challenging chiral primary amines
Nugent, Thomas C.,Negru, Daniela E.,El-Shazly, Mohamed,Hu, Dan,Sadiq, Abdul,Bibi, Ahtaram,Umar, M. Naveed
supporting information; experimental part, p. 2085 - 2092 (2011/10/19)
Difficult-to-access chiral primary amines were formed in good to high yield and ee using a rare example of a one-pot synthesis from prochiral ketones (sequential reductive amination-hydrogenloysis). As a highlight we also demonstrate a one-pot reductive amination-hydrogenolysis-reductive amination (five reactions) of ortho-methoxyacetophenone resulting in the chiral diamine 1-(2-methoxyphenyl)ethyl-(2-pyridylmethyl)-amine (4) (58% overall yield, >99% ee), a new organocatalyst for aqueous enantioselective aldol reactions. Copyright
Cyclohexyl derivatives and their use as therapeutic agents
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Page 21-22, (2010/02/03)
The present invention relates compounds of the formula (I): wherein ring A is a phenyl or pyridyl ring; X represents a linker selected from the group consisting of: (a), (b), (c), (d), (e), (f), (g), (h), (i), (j), (k), (l) and R1, R2, R3, R4, R5, R6, R7, R13, R14, R15, R16, R?17, R18, R19, R21a and R21b are as defined herein. The compounds are of particular use in the treatment or prevention of depression, anxiety, pain, inflammation, migraine, emesis or postherpetic neuralgia.
