470-49-5 Usage
Description
Mesitonic acid, a cyclic dione with the molecular formula C6H6O4 and a molecular weight of 142.11 g/mol, is an organic compound that appears as a yellow solid. It is a strong acid and is soluble in water, ethanol, and other organic solvents. Mesitonic acid is primarily used as a building block in organic chemistry for the synthesis of various other compounds. It is known for its mutagenic and cytotoxic effects and has been studied for its potential applications in medicinal chemistry and material science.
Uses
Used in Pharmaceutical Synthesis:
Mesitonic acid is used as a building block in the synthesis of pharmaceuticals for its ability to form various organic compounds, contributing to the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
Mesitonic acid is used as a key intermediate in organic chemistry for the synthesis of a wide range of compounds, showcasing its versatility and importance in chemical reactions.
Used in Medicinal Chemistry:
Mesitonic acid is used as a starting material in medicinal chemistry, where its mutagenic and cytotoxic properties are harnessed for the development of potential therapeutic agents and treatments.
Used in Material Science:
Mesitonic acid is utilized in material science for its potential applications in creating new materials with unique properties, such as in the development of advanced polymers and composites.
Check Digit Verification of cas no
The CAS Registry Mumber 470-49-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 470-49:
(5*4)+(4*7)+(3*0)+(2*4)+(1*9)=65
65 % 10 = 5
So 470-49-5 is a valid CAS Registry Number.
470-49-5Relevant articles and documents
4-Oxoalkansaeuren, Ester und Amide durch Addition der entsprechenden Enolate an 2-(N-Methylanilino)-acrylonitril
Ahlbrecht, Hubertus,Dietz, Manfred
, p. 417 - 421 (1985)
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Urry,W.H. et al.
, p. 5785 - 5787 (1970)
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Decomposition du percarbonate de O,O-t-butyle et O-isopropenyle en solution: acetonylation des esters, acides et nitriles
Lalande, Robert,Filliatre, Claude,Villenave, Jean-Jacques,Jaouhari, Rabih
, p. 149 - 159 (2007/10/02)
The free-radical decomposition of O,O-t-butyl and O-isopropenyl peroxycarbonate in substrates possessing mobile H-atoms (S-H) consists mainly in an induced chain process leading to acetonylated derivatives of the solvent.Fairly good yields are obtained but the acetonylation of functional substrates often gives mixtures of isomers.In the case of methyl acetate, the acetonylation occurs on the C-atoms adjacent to the carbonyl (acyloxy moiety) and to the O-atom (alkoxy moiety).However, the relative amounts of the isomeric products depend on the concentration of the peroxycarbonate solutions; at lowest concentration, methyl 4-oxopentanoate (acyloxy moiety) is obtained selectively.It is assumed that the free radicals issued from the solvent are able to abstract H-atoms of other molecules of solvent before adding to the double bond of the peroxycarbonate; the more the peroxycarbonate solution is diluted the more the transfers from the C-atom adjacent to the carbonyl to the radicals adjacent to the O-atom are favoured.In the case of methyl alkanoates, H-transfers from the α-C-atoms to β-radicals of the acyloxy moiety may account for the orientation of the process.Owing to similar H-transfer processes, the acetonylation of functional esters, of acids and nitriles is selective in most cases.