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5-phenyl-1,3,5-dithiazixane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142857-79-2

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142857-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142857-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,8,5 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142857-79:
(8*1)+(7*4)+(6*2)+(5*8)+(4*5)+(3*7)+(2*7)+(1*9)=152
152 % 10 = 2
So 142857-79-2 is a valid CAS Registry Number.

142857-79-2Downstream Products

142857-79-2Relevant academic research and scientific papers

Novel synthesis and thermal ring fission of 7-aryl-1,2,3,4,5,7-pentathiazocanes

Shimada, Kazuaki,Yoshida, Takamasa,Makino, Kenshiro,Otsuka, Tatsuya,Onuma, Yuki,Aoyagi, Shigenobu,Takikawa, Yuji,Kabuto, Chizuko

, p. 90 - 91 (2002)

Treatment of 1,5,3,7-dithiadiazocanes 1 with bromine-elemental sulfur or disulfur dichloride (S2Cl2) afforded 1,2,3,4,5,7-pentathiazocanes 3, and heating of 3 caused unusual thermal ring fission to give an inseparable mixture of polysulfide chains bearing a thioformamide moiety on each terminal.

Efficient method for a synthesis of N-substituted dithiazinanes via transamination of N-methyl-1,3,5-dithiazinane with arylamines and hydrazines

Niatshina, Zalifa T.,Murzakova, Natal'ya N.,Vasilieva, Inna V.,Rakhimova, Elena B.,Akhmetova, Vnira R.,Ibragimov, Askhat G.

experimental part, p. 141 - 148 (2011/06/22)

The efficient method for a synthesis of N-substituted dithiazinanes based on the transamination reaction of N-methyl-1,3,5-dithiazinane with arylamines and hydrazines in the presence of Sm and Co catalysts has been developed. ARKAT USA, Inc.

Synthesis, crystal structure, and interconversions of new N-aryl-1,3,5-dithiazinanes, 1,3,5-thiadiazinanes, and 1,5-dithia-3,7- diazacyclooctanes

Akhmetova,Niatshina,Khabibullina,Bushmarinov,Borisova,Starikova,Korzhova,Kunakova

scheme or table, p. 1002 - 1009 (2011/02/26)

Chemoselectivity of multicomponent reaction of anilines with the CH 2O-H2S thiomethylating mixture in the synthesis of N-aryl-substituted 1,3,5-dithiazinanes, 1,3,5-thiadiazinanes, and 1,5-dithia-3,7-diazacyclooctanes has been studied depending on the type and mutual arrangement of substituents in the starting anilines, ratio of reagents, temperature, and reaction time. Conformation of the synthesized heterocycles in crystal has been found by X-ray diffraction. Interconversion of the heterocycles showed stability of N-aryl-1,3,5-dithiazinanes.

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