58291-77-3 Usage
General Description
3-Chloro-5-methylphenol is a synthetic organic compound that falls into the category of phenols and derivatives. These chemicals generally possess antiseptic properties, making them beneficial for use in pharmaceuticals, personal care products, or disinfectant solutions. Some specific applications of 3-Chloro-5-methylphenol could include a role as an intermediate in the production of more complex chemicals or as an active ingredient in pesticide formulations. Its structure contains a chloro group and a methyl group around a central phenol ring. As with many similar compounds, potential risks exist such as skin or eye irritation, and adverse reactions if ingested or inhaled. Recommended handling procedures typically involve the use of protective equipment and ventilation controls.
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 articles and documents
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.
