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2-Butanol, 4,4-bis(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

185559-30-2

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185559-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185559-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,5,5 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 185559-30:
(8*1)+(7*8)+(6*5)+(5*5)+(4*5)+(3*9)+(2*3)+(1*0)=172
172 % 10 = 2
So 185559-30-2 is a valid CAS Registry Number.

185559-30-2Relevant academic research and scientific papers

The effect of hmpa on the reactivity of epoxides, aziridines, and alkyl halides with organolithium reagents

Reich, Hans J.,Sanders, Aaron W.,Fiedler, Adam T.,Bevan, Martin J.

, p. 13386 - 13387 (2002)

A kinetic study of the effect of added HMPA cosolvent on the reaction of 2-lithio-1,3-dithiane (1), bis(phenylthio)methyllithium (2), and bis(3,5-bistrifluoromethylphenylthio)methyllithium (3) with methyloxirane (propylene oxide), N-tosyl-2-methylaziridin

Titanocene(II)-promoted intramolecular olefination of thiol esters: A new route to substituted 2,3-dihydrothiophenes

Rahim, Md. Abdur,Fujiwara, Tooru,Takeda, Takeshi

, p. 1029 - 1032 (2007/10/03)

The treatment of S-[3,3-bis(phenylthio)propyl] thioalkanoates with the low-valent titanium species Cp2Ti[P(OEt)3]2 in THF produced 5-substituted 2,3-dihydrothiophenes in good yields. These thiophene derivatives were found to be susceptible to photoirradiation and easily isomerized into 2-alkylidenetetrahydrothiophenes.

Aggregative activation and carbanion chemistry: Complex base deprotonation and directed functionalisation of dithioacetals

Gros, Philippe,Hansen, Philippe,Caubere, Paul

, p. 15147 - 15156 (2007/10/03)

Bis(phenylthio)methane and [1,3]-dithiane were efficiently deprotonated by the NaNH2-Et(OCH2CH2)2-ONa complex base. A marked behaviour difference was observed between the sodium carbanion of [1,3]-dithiane and the corresponding lithio-derivative. A 'radicaloid' mechanism is proposed to explain the results observed.

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