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75066-24-9

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75066-24-9 Usage

General Description

2-(3,4-DIMETHYL-PHENOXY)-2-METHYL-PROPIONIC ACID is a chemical compound with the molecular formula C13H16O3. It is a derivative of propionic acid and contains a phenyl group with two methyl substituents attached to the four and five positions. 2-(3,4-DIMETHYL-PHENOXY)-2-METHYL-PROPIONIC ACID is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It exerts anti-inflammatory and analgesic effects by inhibiting the production of pro-inflammatory mediators. Additionally, it has been studied for its potential use as a treatment for neurological disorders and as a potential anticancer agent.

Check Digit Verification of cas no

The CAS Registry Mumber 75066-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,6 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75066-24:
(7*7)+(6*5)+(5*0)+(4*6)+(3*6)+(2*2)+(1*4)=129
129 % 10 = 9
So 75066-24-9 is a valid CAS Registry Number.

75066-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-Dimethyl-phenoxy)-2-methyl-propionic acid

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

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

More Details:75066-24-9 SDS

75066-24-9Downstream Products

75066-24-9Relevant articles and documents

The Synthesis of 4-Methylcyclohexa-2,5-dienones from Phenols

Islam, M. Majharul,Waring, Anthony J.

, p. 768 - 783 (2007/10/02)

4-Alkyl phenols have been converted by a known sequence into 2-aryloxyisobutyric acids and thence, by bromination at the 4-position of the aromatic ring with concomitant intramolecular lactone formation, into masked 4-alkyl-4-bromocyclohexa-2,5-dienones.Reaction with lithium dimethylcuprate, as a model for other lithium dialkylcuprates, replaces the bromine by a methyl group.Hydrolytic demasking gives 4-alkyl-4-methylcyclohexa-2,5-dienones.The method should allow the general synthesis of 4-alkylated cyclohexa-2,5-dienones from phenols via a nucleophilic alkylation step.This contrasts with an existing route which uses electrophilic alkylation of phenols or phenoxide ions by a restricted range of reactive alkylating agents.

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