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110668-56-9

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110668-56-9 Usage

General Description

5-Hydroxy-1-(phenylmethyl)-2,4-imidazolindion, also known as tryptophol, is a chemical compound that is derived from the amino acid tryptophan. It is a natural sedative and hypnotic that is produced in the body during the metabolism of tryptophan, and is also found in certain foods such as cheese and fermented beverages. Tryptophol has been shown to have sedative and anticonvulsant effects, and has been used for its calming properties in traditional medicine. It is also a precursor to the neurotransmitter serotonin, which plays a crucial role in regulating mood, sleep, and appetite. Tryptophol has also been studied for its potential therapeutic use in treating anxiety, depression, and insomnia.

Check Digit Verification of cas no

The CAS Registry Mumber 110668-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,6,6 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110668-56:
(8*1)+(7*1)+(6*0)+(5*6)+(4*6)+(3*8)+(2*5)+(1*6)=109
109 % 10 = 9
So 110668-56-9 is a valid CAS Registry Number.

110668-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-5-hydroxyimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4-Imidazolidinedione,5-hydroxy-1-(phenylmethyl)

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:110668-56-9 SDS

110668-56-9Relevant articles and documents

Process for preparing 1-substituted 5-hydroxy-imidazoline-2,4-diones and 1-substituted 5-alkoxy-imidazoline-2,4-diones

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Example 1, (2010/01/31)

A process for preparing specific 1-substituted 5-hydroxy-imidazoline-2,4-diones by reacting glyoxylic acid with N-substituted ureas is provided, where this process is carried out in a 10-80% strength aqueous solution and in the presence of an acid catalyst. The 1-substituted 5-hydroxy-imidazoline-2,4-diones can subsequently be converted in a further reaction step to give 1-substituted 5-alkoxy-imidazoline-2,4-diones.

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