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1-hydroxymethyl-1,2,3,4-tetrahydro-β-carboline is a chemical compound derived from the tetrahydro-β-carboline class of alkaloids, which are naturally occurring in a variety of plants and animals. 1-hydroxymethyl-1,2,3,4-tetrahydro-β-carboline is characterized by its potential neuroactive properties, including neuroprotective and antioxidant effects. Its molecular structure also hints at possible psychoactive properties, which could influence mood and behavior. Further research is essential to explore the full spectrum of physiological impacts and to determine its potential applications in medicinal and neuroscience fields.

21236-66-8

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21236-66-8 Usage

Uses

Used in Pharmaceutical Industry:
1-hydroxymethyl-1,2,3,4-tetrahydro-β-carboline is used as a potential therapeutic agent for neurodegenerative diseases due to its neuroprotective and antioxidant effects. It may help in the treatment of conditions associated with oxidative stress and neuronal damage.
Used in Neuroscience Research:
In the field of neuroscience, 1-hydroxymethyl-1,2,3,4-tetrahydro-β-carboline is utilized for studying its psychoactive properties and potential effects on mood and behavior. This research could lead to a better understanding of the compound's impact on the central nervous system and its possible use in the development of new psychiatric medications.

Check Digit Verification of cas no

The CAS Registry Mumber 21236-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21236-66:
(7*2)+(6*1)+(5*2)+(4*3)+(3*6)+(2*6)+(1*6)=78
78 % 10 = 8
So 21236-66-8 is a valid CAS Registry Number.

21236-66-8Downstream Products

21236-66-8Relevant academic research and scientific papers

Synthesis of 15-azayohimban, a new heterocyclic ring system

Valls,Segarra,Maillo,Bosch

, p. 1065 - 1074 (2007/10/02)

Two synthetic routes to the 15-azayohimban ring system have been studied. The first one, based on a Pictet-Spengler condensation between tryptamine and piperidine acetal 4, gave very low yields of pentacycles 2a. The second, more efficient route involves as the crucial step a cyclization of a N-acyliminium cation generated from imide 11. The different course of the Pictet-Spengler reaction from amino acetals 4 and 8, as compared with amido acetal 7, is discussed.

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