93202-93-8 Usage
Uses
Used in Pharmaceutical Synthesis:
1,2,3,4-tetrahydro-4,6-Isoquinolinediol is used as a precursor in the synthesis of various pharmaceuticals, particularly those targeting the central nervous system. Its chemical properties make it a valuable building block for the development of new drugs with potential therapeutic benefits.
Used in Medical Research:
THIQ is used as a research tool in the study of the biosynthesis of morphine and other opioid alkaloids. Understanding its role in this process can provide insights into the development of new treatments for pain management and addiction.
Used in Drug Addiction Treatment:
1,2,3,4-tetrahydro-4,6-Isoquinolinediol is being researched for its potential as a treatment for drug addiction and dependence. Its psychoactive properties and interaction with the central nervous system suggest that it may have therapeutic applications in managing withdrawal symptoms and reducing cravings.
Used in Neurodegenerative Disease Treatment:
THIQ has demonstrated neuroprotective properties and is being studied for its potential in the treatment of neurodegenerative diseases. Its ability to protect neurons and promote cell survival may contribute to the development of new therapies for conditions such as Alzheimer's and Parkinson's disease.
Used in Drug Delivery Systems:
Due to its controlled status and potential for abuse, THIQ is being incorporated into drug delivery systems to ensure safe and effective administration. These systems aim to optimize the bioavailability and therapeutic outcomes of THIQ while minimizing the risk of misuse.
Check Digit Verification of cas no
The CAS Registry Mumber 93202-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,0 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93202-93:
(7*9)+(6*3)+(5*2)+(4*0)+(3*2)+(2*9)+(1*3)=118
118 % 10 = 8
So 93202-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c11-7-2-1-6-4-10-5-9(12)8(6)3-7/h1-3,9-12H,4-5H2
93202-93-8Relevant academic research and scientific papers
Utilization of a benzyl protective group in the synthesis of tetrahydroisoquinoline derivatives
Alpatova,Yashunskii
, p. 804 - 807 (2007/10/02)
The corresponding N-benzyl-1,2,3,4-tetrahydroisoquinolines, the debenzylation of which is realized by hydrogenation in the presence of Pd black, were synthesized by the reaction of 1-(3-hydroxyphenyl)-2-benzylaminoethanol with aldehydes.
