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1,4-Methanonaphthalene-5,8-dione, 1,4,4a,8a-tetrahydro-6-(phenylthio)-, also known as 6-phenylthio-1,4,4a,8a-tetrahydro-1,4-methanonaphthalene-5,8-dione, is a complex organic compound with the molecular formula C16H14O2S. 1,4-Methanonaphthalene-5,8-dione, 1,4,4a,8a-tetrahydro-6-(phenylthio)- features a naphthalene core with a methyl group (CH3) attached to the 1 and 4 positions, a carbonyl group (C=O) at the 5 and 8 positions, and a phenylthio group (C6H5-S) attached to the 6 position. The compound is characterized by its unique structure, which includes a partially saturated naphthalene ring system and a phenylthio substituent, making it a potential candidate for various chemical and pharmaceutical applications.

95333-41-8

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95333-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95333-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,3 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95333-41:
(7*9)+(6*5)+(5*3)+(4*3)+(3*3)+(2*4)+(1*1)=138
138 % 10 = 8
So 95333-41-8 is a valid CAS Registry Number.

95333-41-8Downstream Products

95333-41-8Relevant academic research and scientific papers

SOME NEW SULFUR AND SELENIUM SUBSTITUTED BENZOQUINONE-CYCLOPENTADIENE DIELS-ALDER ADDUCTS. PART II. MONOSUBSTITUTED ADDUCTS.

Wladislaw, B.,Marzorati, L.,Vitta, C. di,Arruda Campos, I. P. de

, p. 153 - 156 (2007/10/02)

Some new sulfur and selenium monosubstituted benzoquinone-cyclopentadiene Diels-Alder adducts having the endo configuration have been synthesized and characterized.

Lewis Acid Catalyzed Cycloreversion Reaction of Strained Cage Ketones to Triquinane Skeletons: Kinetic Evidence for a Large Acceleration of the Reaction Owing to Stereoelectronic Requirement

Okamoto, Yasushi,Senokuchi, Kazuhiko,Kanematsu, Ken

, p. 4593 - 4599 (2007/10/02)

Cookson's pentacyclic cage diketones substituted with an electron-donating group (1b-e) underwent a remarkably fast cycloreversion reaction under various Lewis acid catalyzed conditions.The high reactivity of these cage ketones is discussed in terms of push-pull type interactions on the basis of large substituent effects and kinetic measurements.Keywords - cycloreversion reaction; Cookson's pentacyclic cage diketone; Lewis acid catalyst; electron-donating group; stereoelectronic effect

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