52222-87-4 Usage
Uses
Used in Chemical Synthesis:
6-Benzoyl-2-naphthol is used as a key intermediate in the synthesis of various chemical compounds, including potassium 6-benzoyl-2-naphthyl sulfate. It serves as a building block for the development of new molecules with potential applications in different fields.
Used in Histochemical Investigations:
6-Benzoyl-2-naphthol is used as a substrate for histochemical investigation of aryl sulfatase activity. Aryl sulfatases are enzymes that catalyze the hydrolysis of sulfate esters, and their activity is essential for various biological processes. By using 6-benzoyl-2-naphthol as a substrate, researchers can study the distribution and activity of these enzymes in tissues and cells.
Used in Histochemical Demonstration of Acid Phosphatase:
6-Benzoyl-2-naphthol is also used in the preparation of substrates for the histochemical demonstration of acid phosphatase in the organs of albino rats. Acid phosphatases are enzymes that catalyze the hydrolysis of phosphate monoesters, and their activity is crucial for various cellular functions. By using 6-benzoyl-2-naphthol as a substrate, researchers can visualize and analyze the distribution and activity of acid phosphatases in different organs, which can provide valuable insights into their role in various physiological and pathological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 52222-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,2 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52222-87:
(7*5)+(6*2)+(5*2)+(4*2)+(3*2)+(2*8)+(1*7)=94
94 % 10 = 4
So 52222-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H12O2/c18-16-9-8-13-10-15(7-6-14(13)11-16)17(19)12-4-2-1-3-5-12/h1-11,18H
52222-87-4Relevant academic research and scientific papers
Pathak, V. P.,Saini, T. R.,Khanna, R. N.
, p. 1269 - 1270 (1983)
Photo-Fries rearrangement of 2-Naphthylbenzoate gives 6-benzoyl-2-naphthol and 8-benzoyl-2-naphthol in addition to the expected product, 1-benzoyl-2-naphthol. - Keywords: Benzoyl-2-naphthols; Photochemistry
α-Nitro-α,β-Unsaturated Ketones: An Electrophilic Acyl Transfer Reagent in Catalytic Asymmetric Friedel-Crafts and Michael Reactions
Parida, Chandrakanta,Maity, Rajendra,Chandra Sahoo, Subas,Chandra Pan, Subhas
supporting information, p. 6700 - 6704 (2019/09/07)
Herein, we introduce α-nitro-α,β-unsaturated ketones as efficient electrophilic acyl transfer reagents, and they were employed in Friedel-Crafts as well as in Michael reactions. The desired acyl transfer products of these reactions were obtained in high yields with high to excellent enantioselectivities with t-leucine-derived squaramide catalyst under mild reaction conditions. Few applications including a synthesis of the isoxazoline motif have been demonstrated.
Photo-Fries reaction of naphthyl esters within zeolites
Pitchumani,Warrier,Cui,Weiss,Ramamurthy
, p. 6251 - 6254 (2007/10/03)
Photolysis of naphthyl esters within zeolites leads to the photo-Fries rearrangements as in isotropic solution. However, a high level of product selectivity is obtained using 'cation as the key'. A key component for predicting the selectivity of photoreactions within zeolites, namely the location of reactants, is missing at this stage.
