58291-77-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloro-5-methylphenol is used as an active ingredient for its antiseptic properties, contributing to the development of pharmaceutical products that require such characteristics.
Used in Personal Care Products:
In the personal care industry, 3-Chloro-5-methylphenol is used as a component in formulations that require antibacterial or antifungal properties to maintain hygiene and prevent infections.
Used in Disinfectant Solutions:
3-Chloro-5-methylphenol is utilized as a key component in disinfectant solutions, where its antiseptic properties help in sanitizing surfaces and reducing the spread of pathogens.
Used as a Chemical Intermediate:
3-Chloro-5-methylphenol serves as an intermediate in the synthesis of more complex chemicals, playing a crucial role in the production of various chemical compounds.
Used in Pesticide Formulations:
3-CHLORO-5-METHYLPHENOL is also used as an active ingredient in pesticide formulations, where its antiseptic properties help in controlling pests and protecting crops.
Check Digit Verification of cas no
The CAS Registry Mumber 58291-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,9 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58291-77:
(7*5)+(6*8)+(5*2)+(4*9)+(3*1)+(2*7)+(1*7)=153
153 % 10 = 3
So 58291-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7ClO/c1-5-2-6(8)4-7(9)3-5/h2-4,9H,1H3
58291-77-3Relevant academic research and scientific papers
Process for the synthesis of phenols from arenes
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Page 22, (2008/06/13)
A process to synthesize substituted phenols such as those of the general formula RR′R″Ar(OH) wherein R, R′, and R″ are each independently hydrogen or any group which does not interfere in the process for synthesizing the substituted phenol including, but not limited to, halo, alkyl, alkoxy, carboxylic ester, amine, amide; and Ar is any variety of aryl or hetroaryl by means of oxidation of substituted arylboronic esters is described. In particular, a metal-catalyzed C—H activation/borylation reaction is described, which when followed by direct oxidation in a single or separate reaction vessel affords phenols without the need for any intermediate manipulations. More particularly, a process wherein Ir-catalyzed borylation of arenes using pinacolborane (HBPin) followed by oxidation of the intermediate arylboronic ester by OXONE is described.
