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3-(2-chlorophenyl)-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73676-89-8

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73676-89-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73676-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,7 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73676-89:
(7*7)+(6*3)+(5*6)+(4*7)+(3*6)+(2*8)+(1*9)=168
168 % 10 = 8
So 73676-89-8 is a valid CAS Registry Number.

73676-89-8Downstream Products

73676-89-8Relevant academic research and scientific papers

One-Pot, Borax-mediated synthesis of structurally diverse N, S-heterocycles in water

Rao, Mugada Sugunakara,Hussain, Sahid

, (2021/05/26)

Herein, a borax–mediated convenient and efficient strategy for the synthesis of prominent structurally diverse N, S-heterocycles such as quinazolin-4(3H)-one, benzothiadiazine 1,1-dioxide, benzothioazole, and benzoxazoles from readily available 2-aminobenzamide/2-aminobenzenesulfonamide/2-aminothiophenol/2-aminophenol with α,α,α-trihalotoluenes at 100 ℃ in water is elaborated. Upon using aldehydes instead of α,α,α-trihalotoluenes, the reactions proceed through domino fashion under the catalytic effect borax to yield 2,3-dihydroquinazolin-4(1H)-one, 3,4-dihydrothiadiazine 1,1-dioxide, and benzothiazoles in one-pot at 60 ℃. The advantages of this protocol are practical simplicity, large substrate scope, moderate to excellent yields, and the use of water as the solvent.

Transition metal-catalyzed C–H functionalization of arylacetic acids for the synthesis of benzothiadiazine 1,1-dioxides

Patil, Bhausaheb N.,Lade, Jatin J.,Karpe, Aniket S.,Pownthurai,Vadagaonkar, Kamlesh S.,Mohanasrinivasan,Chaskar, Atul C.

, p. 891 - 894 (2019/03/05)

Copper-catalyzed practical route for the synthesis of benzothiadiazine 1,1-dioxides has been developed. The method involves C–H functionalization of arylacetic acids to form aromatic aldehydes and their subsequent condensation with 2-aminobenzenesulfonami

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