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2-Propanone,1-(2(3H)-benzothiazolylidene)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15096-91-0

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15096-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15096-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15096-91:
(7*1)+(6*5)+(5*0)+(4*9)+(3*6)+(2*9)+(1*1)=110
110 % 10 = 0
So 15096-91-0 is a valid CAS Registry Number.

15096-91-0Downstream Products

15096-91-0Relevant academic research and scientific papers

Utility of α-Oxoketene Dithioacetal in Organic Synthesis: Synthesis of Some New Spiro (Pyran-4,2'-benzothiazole) Derivatives

El-Sayed, Ahmed Mahmoud,El-Saghier, Ahmed Mohamed Mohamed,Mohamed, Mounir Abbas Ali,El-Shafei, Ahmed Kamal

, p. 605 - 608 (2007/10/03)

Ketene S,S-acetal 1 reacts with 2-aminobenzenethiol to afford 2-(1-acetyl-2-oxopropylidene)benzothiazole 2 which was allowed to react with a variety of active methylene reagents to give spiro derivatives (4-13, 16, 17).Compound 2 also reacts with thiourea, thioacetamide or bromomalononitrile to afford spiro derivatives 14, 15 or spiro 18 through a nucleophilic addition and cyclization.

Synthesis of Acetyl-Substituted Heterocyclic Ketene Aminals and Their Deactylation Reaction

Wang, He-Ting,Wang, Xiao-Jun,Huang, Zhi-Tang

, p. 2141 - 2145 (2007/10/02)

The acetyl-substituted heterocyclic ketene aminals 3-6 were synthesized by the reaction of ketene dithioacetals 2 with diamines.The deacetylation of heterocyclic diacetyl ketene-aminals by alkali was studied, and the corresponding monoacetyl derivatives were studied.

Synthesis, Reactions, and Tautomerism of Ketene N,S-Acetals with Benzothiazoline Ring

Huang, Zhi-Tang,Shi, Xian

, p. 541 - 547 (2007/10/02)

Ketene dithioacetals 2 react with 2-aminothiophenol to afford the corresponding substituted 2(3H)-methylenebenzothiazoles 3.Some compounds 3 react with α,β-unsaturated esters to give 1H-pyridobenzothiazole derivatives 4 and 5 by an electrophilic addition and cyclocondensation sequence.

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