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2'-(2,2-dimethylpropanoyloxy)acetophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135276-49-2

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135276-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135276-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,7 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135276-49:
(8*1)+(7*3)+(6*5)+(5*2)+(4*7)+(3*6)+(2*4)+(1*9)=132
132 % 10 = 2
So 135276-49-2 is a valid CAS Registry Number.

135276-49-2Relevant academic research and scientific papers

Synthesis of Five-, Six-, and Seven-Membered Heterocycles by Intramolecular Ring Opening Reactions of 3-Oxetanol Derivatives

Bach, Thorsten,Kather, Kristian,Kraemer, Oliver

, p. 1910 - 1918 (1998)

Intramolecular ring opening reactions of 2-phenyl-3-oxetanols have been studied. The starting materials were prepared by the photocycloaddition of benzaldehyde and various silyl enol ethers. The intramolecular nucleophile was either incorporated into the silyl enol ether prior to the PaternoBuchi reaction (oxetanes 3,16) or was later installed by functional group interconversion (oxetanes 5, 12). With anionic heteroatom nucleophiles (O, N, S) which were attached to the carbon atom C-3 of the trimethylsilyl-protected oxetanol via an alkyl chain, a substitution at the less substituted position C-4 was observed and the corresponding heterocycles (6, 8, 13, 19) were obtained in moderate to good yields (52-91%). Upon acid catalysis a ring opening of the Boc-protected 3-oxetanol 23 to cyclic carbonates occurred. The reaction did not proceed stereospecifically and resulted in a mixture of diastereomeric products 24 and 25.

Structure-activity relationship studies of flavonoids as potent inhibitors of human platelet 12-hLO, reticulocyte 15-hLO-1, and prostate epithelial 15-hLO-2

Vasquez-Martinez, Yesseny,Ohri, Rachana V.,Kenyon, Victor,Holman, Theodore R.,Sepulveda-Boza, Silvia

, p. 7408 - 7425 (2008/09/18)

Human lipoxygenase (hLO) isozymes have been implicated in a number of disease states and have attracted much attention with respect to their inhibition. One class of inhibitors, the flavonoids, have been shown to be potent lipoxygenase inhibitors but their study has been restricted to those compounds found in nature, which have limited structural variability. We have therefore carried out a comprehensive study to determine the structural requirements for flavonoid potency and selectivity against platelet 12-hLO, reticulocyte 15-hLO-1, and prostate epithelial 15-hLO-2. We conclude from this study that catechols are essential for high potency, that isoflavones and isoflavanones tend to select against 12-hLO, that isoflavans tend to select against 15-hLO-1, but few flavonoids target 15-hLO-2.

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