616-73-9 Usage
Description
3-Methyl-4,6-dinitrophenol is a chemical compound that belongs to the class of dinitrophenols, characterized by their powerful metabolic stimulant properties. It is a potent substance commonly utilized in the production of drugs and explosives, and can also be generated as a byproduct in certain industrial processes. However, it is imperative to note that 3-methyl-4,6-dinitrophenol is highly toxic, posing serious health risks to humans through ingestion, inhalation, or skin absorption, leading to severe symptoms and potentially fatal outcomes.
Uses
Used in Pharmaceutical Production:
3-Methyl-4,6-dinitrophenol is used as a key intermediate in the synthesis of certain pharmaceuticals, owing to its metabolic stimulant properties. Its role in drug production is crucial for the development of medications that target specific metabolic conditions.
Used in Explosive Manufacturing:
This chemical compound is also utilized in the manufacturing of explosives due to its high reactivity and energy content. Its properties make it a valuable component in the production of various explosive materials for both commercial and military applications.
Used in Industrial Processes:
3-Methyl-4,6-dinitrophenol can be generated as a byproduct in certain industrial processes, where its presence may require careful management and disposal to prevent environmental contamination and health hazards.
It is essential to handle, use, and dispose of 3-methyl-4,6-dinitrophenol with extreme caution, adhering to stringent safety guidelines and regulations to mitigate the risks associated with its toxicity.
Check Digit Verification of cas no
The CAS Registry Mumber 616-73-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 616-73:
(5*6)+(4*1)+(3*6)+(2*7)+(1*3)=69
69 % 10 = 9
So 616-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O5/c1-4-2-7(10)6(9(13)14)3-5(4)8(11)12/h2-3,10H,1H3
616-73-9Relevant articles and documents
Highly efficient nitration of phenolic compounds by zirconyl nitrate
Selvam, J. Jon Paul,Suresh,Rajesh,Reddy, S. Ravinder,Venkateswarlu
, p. 2507 - 2509 (2007/10/03)
Zirconyl nitrate was found to be an excellent reagent in the nitration of phenol and substituted phenols to give nitrated phenols. This procedure works efficiently on most of the examples at room temperature yielding nitro derivatives in fair to good yields with high regioselectivity.
Cerium(IV) induced oxidative coupling of simple phenols in the presence and absence of hydrogen peroxide: A comparative study of product distribution
Chakrabarty, Kakoli,Chawla, H. Mohindra,Suresh, Valiya Veettil
, p. 266 - 274 (2007/10/02)
The reaction of cerium(IV) ammonium nitrate with simple phenols (2-, 3- and 4-methylphenols) has been examined in the presence and absence of hydrogen peroxide.It has been observed that though the oxophilicity of cerium(IV) can be controlled by addition of hydrogen peroxide in the reaction medium, there is also a difference in the nature of products formed.The reaction can be used to obtain new terphenyls (3a, 3b and 3e), biphenyls (2a, and 2e), 2-hydroxy-1,9-dimethyl-7-nitro-dibenzyl-p-dioxin (4) and 3,7-dimethyl-1,9-dinitrodibenzofuran (5) in acceptable net yields.
Water-soluble trisazo 8-amino-naphthol-1 dyes
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, (2008/06/13)
Very effective direct dyeing of cotton and other hydroxyl- or nitrogen-containing fibers is effected with water-soluble triasazo dyes having the formula: where A is a radical of a diazoconstituent and A3 is a radical of a coupling constituent STR1 and A1 or A2 or both can have their azo linkages reversed. These dyes are very fast particularly to washing and to perspiration, and are so effective with cotton that dye baths for such use are rapidly exhausted and the disposal of used bath is less of a problem.
