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4-(3-Hydroxy-1,3-diphenyl-propylamino)-benzoic acid methyl ester is a complex organic compound with the molecular formula C23H23NO3. It is a derivative of benzoic acid, featuring a hydroxylated diphenylpropylamine group attached to the 4-position of the benzene ring. This molecule is characterized by its ester functionality, with a methyl group esterifying the carboxylic acid group. It is a white crystalline solid and is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. The compound's structure and properties make it a subject of interest for researchers in medicinal chemistry, given its potential to influence biological activity through its interaction with various receptors and enzymes.

4274-63-9

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4274-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4274-63-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4274-63:
(6*4)+(5*2)+(4*7)+(3*4)+(2*6)+(1*3)=89
89 % 10 = 9
So 4274-63-9 is a valid CAS Registry Number.

4274-63-9Downstream Products

4274-63-9Relevant academic research and scientific papers

Direct introduction of nitrogen and oxygen functionality with spatial control using copper catalysis

Shaum, James B.,Fisher, David J.,Sroda, Miranda M.,Limon, Luis,De Alaniz, Javier Read

, p. 8748 - 8752 (2018/12/10)

Synthetic chemists have spent considerable effort optimizing the synthesis of nitrogen and oxygen containing compounds through a number of methods; however, direct introduction of N- and O-functionality remains challenging. Presented herein is a general method to allow for the simultaneous installation of N- and O-functionality to construct unexplored N-O heterocyclic and amino-alcohol scaffolds. This transformation uses earth abundant copper salts to facilitate the formation of a carbon-centered radical and subsequent carbon-nitrogen bond formation. The intermediate aminoxyl radical is terminated by an intramolecularly appended carbon-centered radical. We have exploited this methodology to also access amino-alcohols with a range of aliphatic and aromatic linkers.

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