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90003-93-3

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90003-93-3 Usage

General Description

2,4-DIMETHYL-6-IODOPHENOL, also known as 2,4-dimethyl-6-iodophenol, is a chemical compound with the molecular formula C8H9IO. It is a derivative of phenol and contains two methyl groups and an iodine atom attached to the benzene ring. This chemical is often used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It has also been studied for its potential antifungal and antibacterial properties, making it a valuable compound for research and development in the fields of medicine and biotechnology. Furthermore, 2,4-DIMETHYL-6-IODOPHENOL is a hazardous chemical and should be handled with appropriate caution and safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 90003-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,0 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90003-93:
(7*9)+(6*0)+(5*0)+(4*0)+(3*3)+(2*9)+(1*3)=93
93 % 10 = 3
So 90003-93-3 is a valid CAS Registry Number.

90003-93-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodo-4,6-dimethylphenol

1.2 Other means of identification

Product number -
Other names 2,4-DIMETHYL-6-IODOPHENOL

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:90003-93-3 SDS

90003-93-3Upstream product

90003-93-3Relevant articles and documents

Gold-catalyzed oxidative acyloxylation of arenes

Pradal, Alexandre,Toullec, Patrick Y.,Michelet, Veronique

experimental part, p. 6086 - 6089 (2011/12/22)

A variety of nonactivated hindered aromatic rings are acyloxylated (22 examples, up to 83% yield) in the presence of PPh3AuCl as the catalyst and di(acetoxy)iodobenzene as the oxidant. The reaction proceeds at 110 °C in an acid media and allows the formation of both hindered acetoxy and acyloxy derivatives. This methodology nicely complements the Pd-catalyzed arene acyloxylation reaction, which is not operating on hindered substrates and allows the Au-catalyzed unprecedented acyloxylation reaction of arenes, implying various carboxylic acids.

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