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4-Benzoyl-4-phenylbutyric acid is a synthetic organic compound with the chemical formula C21H18O4. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 4-Benzoyl-4-phenylbutyric acid is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs. It is characterized by its molecular structure, which includes a butyric acid backbone with a benzoyl group and a phenyl group attached to the fourth carbon. The compound's properties, such as its melting point and solubility, make it a valuable intermediate in the production of certain medications.

4258-41-7

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4258-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4258-41-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4258-41:
(6*4)+(5*2)+(4*5)+(3*8)+(2*4)+(1*1)=87
87 % 10 = 7
So 4258-41-7 is a valid CAS Registry Number.

4258-41-7Relevant academic research and scientific papers

Regioselection in the synthesis of 4-benzyltetral-1-ones and the new 4-arylbenzosuber-1-ones

Truong, Daniel,Howard, Brittany L.,Thompson, Philip E.

, (2021/03/09)

The intramolecular Friedel-Crafts acylation of 4,5-diarylpentanoic acids has the possibility to cyclise to either a 6-membered ring to give 4-benzyltetral-1-one or a 7-membered ring to give 4-arylbenzosuber-1-one. Of these, only the former compound class has previously been reported. The impact of the substituents positioning on the outcome of the cyclisation has been investigated. The complete formation of either the tetralone or the benzosuberone regioisomer was possible under the same reaction conditions, dependent upon the ring activation and/or deactivation of the chosen substituents. Selected bromo or methoxy substituents could be used as auxiliaries, included in precursors to afford the desired regioisomer and then subsequently removed.

Iodine(III)-Mediated Contraction of 3,4-Dihydropyranones: Access to Polysubstituted γ-Butyrolactones

Dagenais, Robin,Lussier, Tommy,Legault, Claude Y.

supporting information, p. 5290 - 5294 (2019/09/03)

Functionalized γ-butyrolactones are privileged structures in the field of medicinal chemistry; they are found in numerous natural products and synthetic compounds with diverse biological activities. The oxidative ring contraction of 3,4-dihydropyran-2-one derivatives represents a promising yet underappreciated strategy to access these compounds. To the best of our knowledge, very few examples of this strategy have been reported, with limited investigation of the influence of stereogenic centers on the starting dihydropyranones. We investigated the iodine(III)-mediated contraction of a representative set of dihydropyranone derivatives. The method gives rapid access to functionalized γ-butyrolactones in good yields. The reaction scope was investigated, and the method was found to support various levels of substituents, even enabling access to sterically congested quaternary centers. The stereoselectivity was investigated using chiral substrates and a chiral iodine(III) reagent.

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