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1-(1,2-dithiocyanatoethyl)-4-methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70372-37-1

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70372-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70372-37-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,7 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70372-37:
(7*7)+(6*0)+(5*3)+(4*7)+(3*2)+(2*3)+(1*7)=111
111 % 10 = 1
So 70372-37-1 is a valid CAS Registry Number.

70372-37-1Downstream Products

70372-37-1Relevant academic research and scientific papers

Hypervalent iodine chemistry: Novel and direct thiocyanation of alkenes using [bis(acetoxy)iodo]benzene/trimethylsilyl isothiocyanate reagent combination. Synthesis of 1,2-dithiocyanates

Bruno, Moira,Margarita, Roberto,Parlanti, Luca,Piancatelli, Giovanni,Trifoni, Maila

, p. 3847 - 3848 (1998)

Novel and direct thiocyanation of alkenes using [bis(acetoxy)iodo]benzene/trimethylsilyl isothiocyanate reagent combination has been developed.

Copper-catalyzed efficient dithiocyanation of styrenes: Synthesis of dithiocyanates

Lv, Yunhe,Pu, Weiya,Cui, Hao,He, Jialin,Zhang, Qinmei

supporting information, p. 1223 - 1229 (2016/08/05)

A novel Cu-catalyzed intermolecular chemoselectivity dithiocyanation of styrenes with ammonium thiocyanate has been developed under mild conditions. This reaction exhibits a wide range of functional-group tolerance in styrenes to afford various dithiocyanates. The reaction mechanism was primarily investigated and a radical process was proposed.

Cis-1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate as an efficient reagent for the synthesis of phenacyl thiocyanates and phenacyl azides

Badri, Rashid,Gorjizadeh, Maryam

experimental part, p. 2058 - 2066 (2012/06/04)

Styrenes efficiently undergo thiocyanation and azidation with cis-1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate at 0C to furnish the corresponding thiocyanatoketones and azidoketones. This method is a direct, one-pot synthesis under mild condition using methanol as solvent.

Ferric(III) chloride-promoted efficient thiocyanation of arylalkenes: A facile synthesis of dithiocyanates

Yadav,Reddy,Gupta, Manoj Kumar

, p. 1983 - 1986 (2007/10/03)

Anhydrous FeCl3 oxidizes potassium thiocyanate to the corresponding radical and promotes subsequent addition to nucleophilic olefins to produce dithiocyanate derivatives under mild conditions with high efficiency. Excellent yields and chemosele

A very efficient Cerium (IV) ammonium nitrate (CAN) mediated thiocyanation of aralkenes: Formation of dithiocyanates

Nair, Vijay,Nair, Latha G.

, p. 4585 - 4586 (2007/10/03)

A facile dithiocyanation of aralkenes mediated by Cerium (IV) ammonium nitrate is described.

Radical additions to olefins in the presence of iodobenzenediacetate: An easy route to alkyl dithiocyanates

De Mico, Antonella,Margarita, Roberto,Mariani, Andrea,Piancatelli, Giovanni

, p. 1889 - 1892 (2007/10/03)

We describe a new application of iodobenzenediacetate (IBDA), which is able to oxidize thiocyanate anion to the corresponding radical. Subsequent addition to nucleophilic olefins leads to dithiocyanate derivatives. The radical addition to olefins is more effective when performing the thiocyanation reaction in presence of Mg(ClO4)2 or TEMPO.

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