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γ-(2-Benzoyloxymethyl-4-methoxy)phenyl-γ-butyrolactone is a complex organic compound with the molecular formula C18H18O6. It is a derivative of γ-butyrolactone, featuring a benzoyloxymethyl group at the 2-position and a methoxy group at the 4-position of the phenyl ring. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving the formation of the lactone ring and subsequent functional group modifications. The compound is of interest to researchers in the field of organic chemistry and drug development due to its structural diversity and potential to be modified for specific therapeutic applications.

87221-53-2

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87221-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87221-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,2 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87221-53:
(7*8)+(6*7)+(5*2)+(4*2)+(3*1)+(2*5)+(1*3)=132
132 % 10 = 2
So 87221-53-2 is a valid CAS Registry Number.

87221-53-2Relevant academic research and scientific papers

Preparation of 5-(2-Benzoyloxymethyl-4-methoxy)phenyl-2(5H)-furanone

Bhat, K. S.,Rao, A. S.

, p. 360 - 364 (2007/10/02)

5-Phenyl-2(5H)-furanone (11), 5-(2-methyl-4-methoxy)phenyl-2(5H)-furanone (16) and 5-(2-benzoyloxymethyl-4-methoxy)phenyl-2(5H)-furanone (6) have been prepared from γ-phenyl-γ-butyrolactone (9), γ-(2-methyl-4-methoxy)phenyl-γ-butyrolactone (14) and γ-(2-benzoyloxymethyl-4-methoxy)phenyl-γ-butyrolactone (4) respectively employing the method of Sharpless. 11 has been converted into 4-oxo-4-phenylbutanoic acid (7) on treatment with alkali.During the Wolff-Kishner reduction of 4-oxo-4-(2-methyl-2-methoxyphenyl)butanoic acid (12) the demethylated product 4-(2-methyl-4-hydroxy)phenylbutanoic acid (19) has also been obtained.

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