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1H-2,1,3-Benzothiadiazine, 3,4-dihydro-4-phenyl-, 2,2-dioxide is a complex organic chemical compound with the molecular formula C10H8N2O3S. It belongs to the class of benzothiadiazine derivatives, which are heterocyclic compounds containing a benzene ring fused to a thiadiazine ring. This specific compound features a dihydro structure, with a phenyl group attached to the 4-position and a dioxide group at the 2,2-position. It is a white crystalline solid and is used in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals and agrochemicals. Due to its complex structure, it is typically synthesized through multi-step reactions involving various reagents and conditions. The compound is also known for its potential biological activities, making it a subject of interest in medicinal chemistry research.

4803-25-2

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4803-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4803-25-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,0 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4803-25:
(6*4)+(5*8)+(4*0)+(3*3)+(2*2)+(1*5)=82
82 % 10 = 2
So 4803-25-2 is a valid CAS Registry Number.

4803-25-2Downstream Products

4803-25-2Relevant academic research and scientific papers

Facile synthesis of 4-substituted 3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2-dioxides

Lee, Chai-Ho,Jin, Guo Fan,Lim, Hyun Wha,Yang, Eun Hye,Lee, Jong-Dae,Nakamura, Hiroyuki,Ban, Hyun Seung,Kang, Sang Ook

experimental part, p. 192 - 197 (2011/10/08)

A new method for the preparation of 4-substituted 3,4-dihydro-1H-2,1,3- benzothiadiazine 2,2-dioxides is described. Treatment of t-butyl N-phenylsulfamoylcarbamate derivatives (1) with different aldehydes afforded the corresponding intramolecular cyclized

Enantioselective synthesis of cyclic sulfamidates via Pd-catalyzed hydrogenation

Wang, You-Qing,Yu, Chang-Bin,Wang, Da-Wei,Wang, Xiao-Bing,Zhou, Yong-Gui

supporting information; experimental part, p. 2071 - 2074 (2009/04/18)

Using Pd(CF3;CO2)2/(S,S)-f-binaphane as the catalyst, an efficient enantioselective synthesis of cyclic sulfamidates was developed via asymmetric hydrogenation of the corresponding cyclic imines in 2,2,2-trifluoroethanol at room temperature with high enantioselectivities (up to 99% ee).

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