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2-Phenyl-7H-<1,2,4>triazolo<5,1-b><1,3>thiazin-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73396-66-4

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73396-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73396-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,9 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73396-66:
(7*7)+(6*3)+(5*3)+(4*9)+(3*6)+(2*6)+(1*6)=154
154 % 10 = 4
So 73396-66-4 is a valid CAS Registry Number.

73396-66-4Downstream Products

73396-66-4Relevant academic research and scientific papers

Reaction of 2-aryl-5-R-5,6-dihydro-7H-[1,2,4]-triazolo[5,1-b][1,3]thiazin- 7-ones with aryl bromomethyl ketones and benzyl bromide

Britsun,Esipenko,Lozinskii

, p. 782 - 786 (2005)

The products of the reaction of 2-aryl-5-R-5,6-dihydro-7H-[1,2,4] triazolo[5,1-b][1,3]thiazin-7-ones with aryl bromomethyl ketones are 2-aryl-7H-[1,2,4]triazolo[5,1-b][1,3]thiazin-7-ones and aryl methyl ketones or 2,5-diaryl[1,3]thiazolo[3,2-b][1,2,4]tria

Regioselective synthesis of 2-substituted [1,2,4]Triazolo[5,1-b][1,3] thiazin-7-ones by heteropolyacids

Motamedi, Radineh,Heravi, Majid M.,Nazari, Zahra,Bamoharram, Fatemeh F.

, p. 1672 - 1675 (2010)

2-Substituted [1,2,4]triazolo[5,1-b][1,3]thiazin-7-ones 3 were synthesized via regioselective cyclization of 4H-[1,2,4]triazol-3-ylsulfanyl-acrylic acids 2 in the presence of catalytic amounts of heteropolyacids at room temperature in very good yields and

Sulfuric acid: A mild catalyst for the regioselective synthesis of 2-substituted [1,2,4]triazolo[5,1- b][1,3]thiazin-7-ones

Heravi,Montazeri,Rahimizadeh,Bakavoli,Ghassemzadeh

, p. 1225 - 1228 (2001)

A facile and regioselective synthesis of 2-substituted [1,2,4]triazolo[5,1-b][1,3]thiazin-7-ones by action of sulfuric acid on (4H-[1,2,4]triazol-3-ylsulfanyl)-acrylic acids is described.

Synthesis of 1,2,4-triazolo[5,1-b][1,3]-thiazin-7-ones catalyzed by pentafluorophenylammonium triflate

Montazeri,K. Pourshamsian,A. Divsalar,M. Ghoorchi-Beigi

experimental part, p. 2802 - 2804 (2012/08/28)

Pentafluorophenylammonium triflate has been found to be an outstanding catalyst for the cyclization of 3-(4H-1,2,4-triazol-3-ylsulfanyl)- acrylic acids into 1,2,4-triazolo[5,1-b][1,3]thiazin-7-ones under solvent-free microwave irradiation and conventional

Sulfuric acid impregnated on silica gel (H2SO 4/SiO2): A versatile and reusable catalyst for the synthesis of 1,2,4-Triazolo[5,1-b][1,3]thiazin-7-ones

Montazeri

experimental part, p. 7432 - 7434 (2012/06/30)

Sulfuric acid adsorbed on silica gel (H2SO4/SiO 2) has been found to be a highly efficient and versatile catalyst for the cyclization of 3-(4H-1,2,4-triazol-3-ylsulfanyl)-acrylic acids into 1,2,4-triazolo[5,1-b][1,3]- thia

7H-Triazolothiazin-7-ones by Deamination Cyclization of S-Acrylates of 4-Amino-3(3H)-1,2,4-triazolethiones

Heindel, Ned D.,Reid, Jack R.

, p. 2479 - 2482 (2007/10/02)

Condensation of 4-amino-3(3H)-1,2,4-triazolethiones with methyl propiolate gave S-acrylic esters.S-Acrylic acids prepared from these esters underwent a deamination cyclization of 7H-triazolothiazin-7-ones with the loss of the elements o

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