Welcome to LookChem.com Sign In|Join Free
  • or
Carbomethoxyibogamine hydrochloride is a synthetic derivative of ibogaine, a naturally occurring psychoactive alkaloid found in the root bark of the Tabernanthe iboga plant. It is a potent hallucinogenic and psychoactive drug that primarily affects the central nervous system. CARBOMETHOXYIBOGAMINE HYDROCHLORIDE is often utilized in research to explore its potential therapeutic effects on various conditions, including addiction and depression. Additionally, it is employed in some alternative medicine practices for its purported spiritual and psychological healing properties. However, due to its potential for abuse and the absence of approved medical uses, carbomethoxyibogamine hydrochloride is classified as a Schedule I controlled substance in the United States.

4503-12-2

Post Buying Request

4503-12-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4503-12-2 Usage

Uses

Used in Pharmaceutical Research:
Carbomethoxyibogamine hydrochloride is used as a research chemical for investigating its potential therapeutic effects on various conditions. It is particularly studied for its effects on the central nervous system and its potential to treat addiction and depression.
Used in Alternative Medicine Practices:
In some alternative medicine practices, carbomethoxyibogamine hydrochloride is used as a spiritual and psychological healing agent. It is believed to offer profound insights and self-reflection, contributing to personal growth and transformation.

Check Digit Verification of cas no

The CAS Registry Mumber 4503-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,0 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4503-12:
(6*4)+(5*5)+(4*0)+(3*3)+(2*1)+(1*2)=62
62 % 10 = 2
So 4503-12-2 is a valid CAS Registry Number.

4503-12-2Downstream Products

4503-12-2Relevant academic research and scientific papers

Synthesis of (-)-pseudotabersonine, (-)-pseudovincadifformine, and (+)-coronaridine enabled by photoredox catalysis in flow

Beatty, Joel W.,Stephenson, Corey R. J.

, p. 10270 - 10273 (2014/08/05)

Natural product modification with photoredox catalysis allows for mild, chemoselective access to a wide array of related structures in complex areas of chemical space, providing the possibility for novel structural motifs as well as useful quantities of less abundant congeners. While amine additives have been used extensively as stoichiometric electron donors for photocatalysis, the controlled modification of amine substrates through single-electron oxidation is ideal for the synthesis and modification of alkaloids. Here, we report the conversion of the amine (+)-catharanthine into the natural products (-)-pseudotabersonine, (-)-pseudovincadifformine, and (+)-coronaridine utilizing visible light photoredox catalysis.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 4503-12-2