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5-Benzyloxyindole-3-glyoxylylamide is a chemical compound that serves as an intermediate in the synthesis of hydroxyindolylglyoxylic acid amides and serotonin derivatives. It is characterized by its yellow powder form and is utilized in various applications across different industries due to its unique chemical properties.

22424-62-0

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22424-62-0 Usage

Uses

Used in Pharmaceutical Industry:
5-Benzyloxyindole-3-glyoxylylamide is used as an intermediate for the synthesis of hydroxyindolylglyoxylic acid amides, which are important compounds in the development of pharmaceuticals. These amides have potential applications in the treatment of various medical conditions, making 5-Benzyloxyindole-3-glyoxylylamide a valuable component in the pharmaceutical industry.
Used in Chemical Research:
As an intermediate in the preparation of serotonin derivatives, 5-Benzyloxyindole-3-glyoxylylamide plays a crucial role in chemical research. Serotonin is a neurotransmitter that has been linked to various physiological and psychological processes, including mood regulation, appetite, and sleep. The compound's involvement in the synthesis of serotonin derivatives makes it an essential tool for researchers studying the effects and potential applications of serotonin in the field of neuroscience and mental health.

Check Digit Verification of cas no

The CAS Registry Mumber 22424-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22424-62:
(7*2)+(6*2)+(5*4)+(4*2)+(3*4)+(2*6)+(1*2)=80
80 % 10 = 0
So 22424-62-0 is a valid CAS Registry Number.

22424-62-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-2-(5-phenylmethoxy-1H-indol-3-yl)acetamide

1.2 Other means of identification

Product number -
Other names 5-benzyloxy-3-indoleglyoxylamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22424-62-0 SDS

22424-62-0Relevant academic research and scientific papers

A deuterium generation 5- hydroxy primary color ammonia xylosides derivative and its preparation method

-

Paragraph 0040; 0042-0044, (2017/04/11)

The invention discloses deuterated 5-hydroxy tryptophan glucoside derivatives and a preparation method thereof. The preparation method comprises the following steps: first, with 5-benzyloxyindole as an initial material, carrying out acylation reaction and

A versatile linkage strategy for solid-phase synthesis of N,N-dimethyltryptamines and β-carbolines

Wu, Tom Y. H.,Schulte, Peter G.

, p. 4033 - 4035 (2007/10/03)

(matrix presented) Various tryptamines are captured by a vinylsulfonylmethyl polystyrene resin, generating a safety-catch linkage. β-Carbolines can be formed from 4 by a Pictet-Spengler reaction with the introduction of R1. Tryptamine 4 can also be derivatized by acylation or copper-mediated coupling to introduce R2. If X = Br, Suzuki coupling can be used to introduce R3. After derivatization, the indole derivatives are activated with methyl iodide and released under mild basic condition.

The synthesis of alpha, alpha, beta, beta-d4-serotonin.

Shaw,Wright,Milne

, p. 146 - 148 (2007/10/08)

Alpha, alpha, beta, beta-d4-Serotonin (94% d4, 6% d3) has been synthesized for use as an internal standard in mass spectrometric determinations of serotonin in biological systems.

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