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2-Cyclohepten-1-one, 2-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85808-24-8

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85808-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85808-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,0 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85808-24:
(7*8)+(6*5)+(5*8)+(4*0)+(3*8)+(2*2)+(1*4)=158
158 % 10 = 8
So 85808-24-8 is a valid CAS Registry Number.

85808-24-8Relevant academic research and scientific papers

Iodine-catalyzed selective synthesis of 2-sulfanylphenols via oxidative aromatization of cyclohexanones and disulfides

Ge, Wenlei,Zhu, Xun,Wei, Yunyang

supporting information, p. 3014 - 3021 (2014/03/21)

Iodine-catalyzed intermolecular dehydrogenative aromatizations of six-membered cyclohexanones for the selective synthesis of 2-sulfanylphenols have been developed. Both aryl and alkyl disulfides can be used as sulfanylation reagents to give the desired pr

Cyclopentannulations Leading to the Synthesis of Bicyclic Conjugated Enediones

Yechezekel, Tamar,Ghera, Eugene,Ostercamp, Daryl,Hassner, Alfred

, p. 5135 - 5142 (2007/10/02)

Base-induced reactions of 1-(phenylsulfonyl)-2-methylene-3-bromopropane (4) with 2-(phenylsulfonyl)-2-cycloalkenones 8a-d were investigated with the ultimate purpose to develop a route leading to bicyclic conjugated enediones.Low-temperature, fast-quenche

CARBENOID TYPE BASE INDUCED RING EXPANSION OF THE ADDUCTS OF CYCLIC KETONES WITH BIS(PHENYLTHIO)METHYLLITHIUM

Abraham, William D.,Bhupathy, M.,Cohen, Theodore

, p. 2203 - 2206 (2007/10/02)

In another application of the principle that metallo derivatives of bis(phenylthio)acetals behave as carbenoids when present in the same molecule with another anionic group, the adducts of cyclic ketones with bis(phenylthio)methyllithium react with an alk

REGIOSPECIFIC SYNTHESIS OF α-(PHENYLTHIO)CYCLOALKENONES AND OF α-PHENYL-α-(PHENYLTHIO)KETONES VIA αα-ADDITION OF PHENYLSULPHENYL CHLORIDE TO α-DIAZOKETONES

McKervey, M. Anthony,Ratananukul, Piniti

, p. 117 - 120 (2007/10/02)

Cyclic α-diazoketones react with phenylsulphenyl chloride at room temperature to furnish α-chloro-α-(phenylthio)cycloalkanones which undergo ready dehydrochlorination to α-(phenylthio)cycloalkenones when treated with triethylamine; acyclic, terminal α-diazoketones also furnish α-chloro-α-(phenylthio)adducts which are useful electrophiles in the synthesis of α-phenyl-α-(phenylthio)ketones.

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