148324-47-4 Usage
Molecular structure
Consists of a benzyl group attached to a phenyl ring, an ethene molecule, and another phenyl ring with a hydroxy group and an ethoxycarbonyl group attached.
Potential applications
Organic chemistry building block, synthesis of more complex compounds, pharmaceutical industry, and research as a reagent or intermediate for the production of other chemical compounds.
Functional groups
Benzyl, phenyl, ethene, hydroxy, and ethoxycarbonyl groups.
Chemical properties
May undergo addition reactions due to the presence of the ethene molecule, and may react with other compounds through its hydroxy and ethoxycarbonyl groups.
Physical properties
The physical properties of 2-(4'-benzyloxyphenyl)-1-(3-hydroxy-2-ethoxycarbonylphenyl)ethene are not explicitly mentioned in the material provided, but it may have characteristics such as melting point, boiling point, and solubility that can be determined through experimental analysis.
Reactivity
The compound may be reactive due to the presence of various functional groups, which can participate in different chemical reactions and form new bonds with other compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 148324-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,3,2 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 148324-47:
(8*1)+(7*4)+(6*8)+(5*3)+(4*2)+(3*4)+(2*4)+(1*7)=134
134 % 10 = 4
So 148324-47-4 is a valid CAS Registry Number.
148324-47-4Relevant academic research and scientific papers
Efficient syntheses of (+/-)-hydrangenol, (+/-)-phyllodulcin and (+/-)-macrophyllol
Guenes, Mehmet,Speicher, Andreas
, p. 8799 - 8802 (2007/10/03)
In this paper we report on a efficient and flexible synthetic route towards the total syntheses of the dihydrocoumarine derivatives hydrangenol (1), phyllodulcin (1a) and macrophyllol (6b). The syntheses started with a readily available phosphonium salt 2 and suitable modified benzaldehydes 3/3a/3b resulting in 46 to 61 percent overall yields in three to four-steps sequences. The racemic products could be separated by chiral HPLC. The evidence of the (R)-enantiomer for sweetness could be demonstrated for 1a.
