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3-(3-chlorophenyl)-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide is a complex organic chemical compound with the molecular formula C14H12ClNOS2. It is a derivative of benzo[e][1,2,4]thiadiazine, which is a fused ring system consisting of a benzene ring attached to a 1,2,4-thiadiazine ring. The compound features a 3-chlorophenyl group attached to the benzene ring, and it exists in a 3,4-dihydro form, indicating the presence of two hydrogen atoms in the molecule. The 1,1-dioxide functional group suggests the presence of two oxygen atoms bonded to the sulfur atom in the thiadiazine ring. 3-(3-chlorophenyl)-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide may have potential applications in pharmaceuticals or as a chemical intermediate due to its unique structure and properties.

3306-83-0

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3306-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3306-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3306-83:
(6*3)+(5*3)+(4*0)+(3*6)+(2*8)+(1*3)=70
70 % 10 = 0
So 3306-83-0 is a valid CAS Registry Number.

3306-83-0Downstream Products

3306-83-0Relevant academic research and scientific papers

Preparation method of benzothiadiazine-1, 1-dioxide compound

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Paragraph 0085-0089, (2021/07/17)

The invention relates to a synthesis method of a benzothiadiazine-1, 1-dioxide compound, and develops a novel solvent-free synthesis method of the benzothiadiazine-1, 1-dioxide compound. No solvent is added in the reaction process, and even part of the product can be obtained through separation without post-treatment. Therefore, the separation and purification process of the product is easy to implement, the reaction time is shortened, the yield of the product is increased, the yield can reach 73%-98%, the purity can reach 96%-99%, the use of toxic solvents is reduced to the greatest extent, and the problems of resource waste, environmental pollution and the like caused by the solvents are fundamentally solved. The method thoroughly eliminates the heavy metal pollution problem in the product from the source, is suitable for preparation of active pharmaceutical ingredients (API), biological agents and the like, and meets the requirements of green chemistry concept.

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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