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2,6-dihydroxyenzeneacetamide is a chemical compound with the molecular formula C8H9NO3. It is an aromatic compound derived from acetamide, featuring a benzene ring with two hydroxyl groups at the 2nd and 6th positions. 2,6-dihydroxyenzeneacetamide is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates. Due to its hydroxyl groups, it can participate in a range of chemical reactions, such as esterification, etherification, and condensation reactions. The compound's properties, such as solubility and reactivity, can be influenced by the presence of these functional groups, making it a versatile building block in organic chemistry.

5663-54-7

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5663-54-7 Usage

Derivative of

Acetaminophen

Usage

Intermediate in the synthesis of pharmaceuticals

Contains

Two hydroxyl groups and an amide group

Building block for

Various organic chemical reactions

Exhibits

Analgesic and antipyretic properties

Similar to

Acetaminophen in its effects

Used as

Precursor in the production of drugs for pain relief and fever reduction

Studied for

Potential antioxidant and anti-inflammatory properties

Value in

Medicinal and pharmaceutical research

Check Digit Verification of cas no

The CAS Registry Mumber 5663-54-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5663-54:
(6*5)+(5*6)+(4*6)+(3*3)+(2*5)+(1*4)=107
107 % 10 = 7
So 5663-54-7 is a valid CAS Registry Number.

5663-54-7SDS

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 Homogentisinsaeureamid

1.2 Other means of identification

Product number -
Other names -

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:5663-54-7 SDS

5663-54-7Upstream product

5663-54-7Relevant academic research and scientific papers

Synthesis of 5-hydroxyoxaindan-2-ones and indol-5-ols from 1,4- cyclohexanedione

Ozaki, Yutaka,Quan, Zhe-Shan,Watabe, Kyouko,Kim, Sang-Won

, p. 727 - 731 (2007/10/03)

1,4-Cyclohexanedione reacted with 2-oxocarboxylic acids to give 5- hydroxyoxaindan-2-ones including homogentisic lactone in one pot. The obtained aromatic compounds were transformed into indol-5-ols in a few steps. The sequential reactions showed a significance of 1,4-cyclohexanedione as a starting material in aromatic synthesis and an alternative access to the indol-5-ols.

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