7472-38-0 Usage
Chemical structure
1-(biphenyl-4-yl)-2-hydroxy-2-methylpropan-1-one is a ketone derivative with a biphenyl group attached to a 2-hydroxy-2-methylpropan-1-one moiety.
Functional groups
The compound contains a ketone group (C=O), a hydroxyl group (-OH), and a methyl group (-CH3).
Molecular weight
Approximately 238.29 g/mol
Physical state
Likely a solid at room temperature, based on its molecular weight and structure.
Solubility
The compound may be soluble in organic solvents such as ethanol, methanol, or acetone, due to its nonpolar and polar functional groups.
Reactivity
As a ketone derivative, it may undergo reactions such as nucleophilic addition, reduction, and oxidation.
Potential applications
The compound may have potential uses in the pharmaceutical or chemical industries due to its unique structure and properties.
Further research
Additional research and testing are required to fully understand the compound's potential uses, effects, and safety.
Safety precautions
As with any new chemical compound, appropriate safety measures should be taken when handling and studying 1-(biphenyl-4-yl)-2-hydroxy-2-methylpropan-1-one, including the use of personal protective equipment and proper disposal methods.
Check Digit Verification of cas no
The CAS Registry Mumber 7472-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7472-38:
(6*7)+(5*4)+(4*7)+(3*2)+(2*3)+(1*8)=110
110 % 10 = 0
So 7472-38-0 is a valid CAS Registry Number.
7472-38-0Relevant articles and documents
Ozonolysis of enol ethers. Part 8. Ozonation of (1-methoxy-2-methylprop-1-enyl)-1,1′-biphenyl in comparison with related oxygenations
Schank, Kurt,Weiter, Matthias
, p. 2105 - 2124 (2007/10/03)
The results of conversions of 4-(1-methoxy-2-methylprop-1-enyl)-1,1′-biphenyl (19) with ozone and with dimethyldioxirane (6b) under 'normal' and 'inverse' conditions are compared with oxygenations by dioxygen under thermal and sensitized photochemical conditions, as well as with the photooxygenation of epoxide 17, formally derived from 19. Ozone consumption varies between 0.7 and 1 mol-equiv. amounts, peroxidic species are not formed. Except for bicyclus 24, ali conversions lead to mixtures of the same [1,1′-biphenyl]-4-yl compounds which only differ by varying percentages. It is concluded that ozonolysis of C=C bonds only represents a special type of electron-transfer oxygenation.
