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(4-Methoxy-phenyl)-acetic acid o-tolyl ester, also known as 2-methoxyphenyl 2-(4-methoxyphenyl)acetate, is an organic compound with the chemical formula C15H16O4. It is a derivative of phenylacetic acid, featuring a 4-methoxyphenyl group attached to the phenyl ring of the acetic acid moiety, and an o-tolyl (2-methylphenyl) group esterified to the carboxylic acid group. (4-Methoxy-phenyl)-acetic acid o-tolyl ester is characterized by its aromatic structure and ester functionality, which may contribute to its potential applications in chemical synthesis or as an intermediate in the preparation of more complex molecules. The presence of methoxy groups on the phenyl rings can influence its reactivity and physical properties, such as solubility and boiling point.

74384-22-8

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74384-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74384-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,8 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74384-22:
(7*7)+(6*4)+(5*3)+(4*8)+(3*4)+(2*2)+(1*2)=138
138 % 10 = 8
So 74384-22-8 is a valid CAS Registry Number.

74384-22-8Relevant academic research and scientific papers

Fries Rearrangement of ortho- and para-Methoxy Phenyl Acetates. The formation of Ketoesters

Martin, Robert,Gros, Nicole,Boehmer, Volker,Kaemmerer, Hermann

, p. 81 - 92 (2007/10/02)

During the Fries rearrangement of o- and p-methoxy phenyl acetates with AlCl3 in nitromethane at 20 deg C substitution occurs mainly in the p-position of the phenolic residue to yield p-acylphenols.Larger quantities of o-acylphenols are obtained only, if

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