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65817-24-5

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65817-24-5 Usage

Explanation

The compound is also referred to as Famprofazone in the field of pharmaceuticals and medicine.

Explanation

2-(4-Methyl-2-hydroxyphenyl)propionic acid gamma-lactone belongs to the class of propionic acids, which are a group of organic compounds.

Explanation

It is a lactone derivative, which means it has a cyclic ester structure in its molecular composition.

Explanation

The compound has been studied for its potential to relieve pain (analgesic) and reduce inflammation (anti-inflammatory) in the body.

Explanation

Famprofazone has been investigated for its ability to inhibit the formation of prostaglandins, which are chemicals that play a role in the body's inflammatory response.

Explanation

The compound has been studied for its potential to effectively relieve pain in various conditions.

Explanation

2-(4-Methyl-2-hydroxyphenyl)propionic acid gamma-lactone is used in the synthesis of various pharmaceuticals and research chemicals, contributing to the development of new medications.

Chemical class

Propionic acids

Structure

Lactone derivative

Pharmaceutical applications

Potential analgesic and anti-inflammatory properties

Inhibition of prostaglandins

Involved in inflammatory response

Pain relief

Potential as an effective pain reliever

Synthesis

Pharmaceutical and research chemicals

Check Digit Verification of cas no

The CAS Registry Mumber 65817-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,1 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65817-24:
(7*6)+(6*5)+(5*8)+(4*1)+(3*7)+(2*2)+(1*4)=145
145 % 10 = 5
So 65817-24-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c1-6-3-4-8-7(2)10(11)12-9(8)5-6/h3-5,7H,1-2H3

65817-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dimethyl-3H-1-benzofuran-2-one

1.2 Other means of identification

Product number -
Other names Dimethyl-3,6-benzo-2(3H)-furanone

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:65817-24-5 SDS

65817-24-5Relevant articles and documents

Synthesis of Benzofuranones via Palladium-Catalyzed Intramolecular Alkoxycarbonylation of Alkenylphenols

Hirschbeck, Vera,Fleischer, Ivana

supporting information, p. 2854 - 2857 (2018/02/06)

Herein, a new catalytic system to synthesize benzofuranones is reported. A palladium-catalyzed intramolecular alkoxycarbonylation is employed to generate 3-substituted-benzofuran-2(3H)-ones from alkenylphenols under mild reaction conditions, linked to an ex situ formation of CO from N-formylsaccharin. The carefully chosen catalytic system enables an efficient reaction with a novel functional group tolerance, despite the high polymerization tendency of the starting material.

Use of 3,6-dimethyl-2(3H)-benzofuranone as flavor material and new process for its preparation

-

, (2008/06/13)

3,6-Dimethyl-2(3H)-benzofuranone is a new, valuable flavor material. A process for its industrial-scale preparation was developed.

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