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lithium 4-(methyl)dithiobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74670-37-4

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74670-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74670-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,7 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74670-37:
(7*7)+(6*4)+(5*6)+(4*7)+(3*0)+(2*3)+(1*7)=144
144 % 10 = 4
So 74670-37-4 is a valid CAS Registry Number.

74670-37-4Downstream Products

74670-37-4Relevant academic research and scientific papers

Preparation and Some Reactions of Thioacyl Diphenylthiophosphinoyl and Thioacyl Diphenylphosphino Sulfides

Kato, Shinzi,Goto, Masahisa,Hattori, Rikizoh,Nishiwaki, Koh-ichi,Mizuta, Masateru,Ishida, Masaru

, p. 1668 - 1683 (2007/10/02)

The reaction of sodium or caesium dithiocarboxylates with diphenylthiophosphinic and diphenylselenophosphinic chlorides gives purple thioacyl diphenylthiophosphinoyl 5 and dark green thioacyl diphenylselenophosphinoyl sulfides 6, which are useful thioacylating reagents under mild reaction conditions.Thioacyl diphenylphosphino sulfides 22, which can be obtained by the similar method using diphenylphosphinous chlorides, react with methanol to yield the corresponding methyl dithiocarboxylates 15, while the reactions of 22 with N-chlorosuccinimide lead to hitherto unknown N-(thioacetylthio)succinimides 28.

The Preparation and Some Reactions of Unsymmetrical Acyl Thioacyl Sulfides

Kato, Shinzi,Sugino, Katsumi,Matsuzawa, Yukihiko,Katada, Tomonori,Noda, Ippei,et al.

, p. 1798 - 1811 (2007/10/02)

A number of unsymmetrical acyl thioacyl sulfides have been prepared and characterized by the reaction of piperidinium or sodium dithiocarboxylates with acyl chlorides or by desulfurization reaction of acyl thioacyl disulfides with triphenylphosphine.They are deep blue oils or light green crystals and very unstable thermally and for moisture.The n --> ?* transitions of the thiocarbonyl group of 1 appear in higher wave length region than those of the corresponding symmetrical bis(thioacyl) sulfides .Some reactions with nucleophiles are discussed.It was found that the symmetricallization reaction of these unsymmetrical acyl thioacyl sulfides occurs in the presence of base such as lithium ethanethiolate to give the symmetrical bis(thioacyl) disulfides in fair yield.

A Convenient Preparation Method of Anhydrous Lithium, Potassium, Rubidium and Cesium Dithiocarboxylates

Kato, Shinzi,Yamada, Shunji,Goto, Hideyuki,Terashima, Kiyomitsu,Mizuta, Masateru,Katada, Tomonori

, p. 458 - 462 (2007/10/02)

It has been found that a series of anhydrous alkali metal dithiocarboxylates are readily obtained in good yields by the reaction of dithio acid with metal hydride (LiH, NaH, KH), n-butyl lithium, or rubidium or cesium acetates, respectively.Their spectral

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