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γ-(2-Methyl-4-methoxy)phenyl-α-phenylseleno-γ-butyrolactone is a complex organic compound characterized by its unique molecular structure. It features a γ-butyrolactone ring, which is a four-membered lactone ring, and is further distinguished by the presence of a phenylseleno group (a phenyl ring bonded to a selenium atom) and a 2-methyl-4-methoxyphenyl group. γ-(2-Methyl-4-methoxy)phenyl-α-phenylseleno-γ-butyrolactone is known for its potential applications in the field of organic synthesis and may have implications in pharmaceutical research due to its selenium-containing structure, which can influence biological activity. The specific arrangement of functional groups in this molecule can affect its reactivity and stability, making it a subject of interest for chemists studying the properties and potential uses of complex organic molecules.

87221-49-6

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87221-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87221-49-6 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, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87221-49:
(7*8)+(6*7)+(5*2)+(4*2)+(3*1)+(2*4)+(1*9)=136
136 % 10 = 6
So 87221-49-6 is a valid CAS Registry Number.

87221-49-6Relevant 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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