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(R)-3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid is a chiral organic compound with the molecular formula C12H16O4. It features a 2-methylpropanoic acid backbone, which is a three-carbon chain with a carboxyl group at one end and a methyl group at the other. The 3,4-dimethoxyphenyl group is attached to the third carbon of the propanoic acid chain, providing two methoxy substituents on the phenyl ring at the third and fourth positions. (R)-3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid is a specific enantiomer, with the "R" designation indicating the configuration of the chiral center. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties.

7306-32-3

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7306-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7306-32-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7306-32:
(6*7)+(5*3)+(4*0)+(3*6)+(2*3)+(1*2)=83
83 % 10 = 3
So 7306-32-3 is a valid CAS Registry Number.

7306-32-3Relevant academic research and scientific papers

Concise synthesis of 2-benzazepine derivatives and their biological activity

So, Masahiro,Kotake, Tomoko,Matsuura, Kenji,Inui, Makoto,Kamimura, Akio

, p. 4017 - 4028 (2012/06/15)

Figure Persented: 2-Benzazepines, which are potentially good candidates for new drug therapies to treat skin wounds, were readily prepared from substituted cinnamylamide via an intramolecular Friedel-Crafts reaction. With few steps and effective reactions

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