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Ethanone, 1-(3,4-dihydroxyphenyl)-2-[methyl(phenylmethyl)amino]-, methanesulfonate (salt) is a complex organic chemical compound characterized by the presence of a ketone group, a dihydroxyphenyl ring, and a methylated phenylmethyl amino group. Ethanone, 1-(3,4-dihydroxyphenyl)-2-[methyl(phenylmethyl)amino]-,methanesulfonate (salt) is typically encountered as a methanesulfonate salt, which contributes to its solubility and reactivity in various chemical processes. Its unique structure endows it with potential biological activities and medicinal properties, positioning it as a significant entity in pharmaceutical research and development.

30392-46-2

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30392-46-2 Usage

Uses

Used in Pharmaceutical Research and Development:
Ethanone, 1-(3,4-dihydroxyphenyl)-2-[methyl(phenylmethyl)amino]-, methanesulfonate (salt) serves as a valuable reagent or intermediate in the synthesis of a range of organic compounds with potential therapeutic applications. Its unique chemical structure allows for the exploration of new drug candidates, particularly those targeting specific biological pathways or receptors.
Used in Chemical Synthesis:
In the chemical synthesis industry, Ethanone, 1-(3,4-dihydroxyphenyl)-2-[methyl(phenylmethyl)amino]-,methanesulfonate (salt) is utilized as a key intermediate for creating various complex organic molecules. Its versatility in forming different chemical bonds and its stability under certain reaction conditions make it an essential component in the production of specialty chemicals and pharmaceuticals.
Used in Drug Discovery:
Due to its potential biological activities, Ethanone, 1-(3,4-dihydroxyphenyl)-2-[methyl(phenylmethyl)amino]-, methanesulfonate (salt) is employed in drug discovery processes. It may be tested for its effects on different biological systems, providing insights into its possible use as a lead compound for the development of new medications.
Used in Analytical Chemistry:
Ethanone, 1-(3,4-dihydroxyphenyl)-2-[methyl(phenylmethyl)amino]-,methanesulfonate (salt) may also find applications in analytical chemistry as a standard or reference material for the development and validation of analytical methods. Its distinct chemical properties can be leveraged to calibrate instruments and establish protocols for the analysis of similar compounds in complex mixtures.

Check Digit Verification of cas no

The CAS Registry Mumber 30392-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,9 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30392-46:
(7*3)+(6*0)+(5*3)+(4*9)+(3*2)+(2*4)+(1*6)=92
92 % 10 = 2
So 30392-46-2 is a valid CAS Registry Number.

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