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2-((phenylsulfonyl)methyl)benzo[d]thiazole is a complex organic chemical compound characterized by a benzo[d]thiazole ring, which is a fused ring system consisting of a benzene ring and a thiazole ring. The molecule features a phenylsulfonyl group attached to the benzo[d]thiazole through a methylene bridge. This specific arrangement of atoms and functional groups endows the compound with unique chemical properties, making it potentially useful in various applications such as pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of other complex molecules. The compound's structure provides a balance of aromaticity, sulfur, and sulfonyl functionalities, which can influence its reactivity and stability in different chemical environments.

53803-98-8

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53803-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53803-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,0 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53803-98:
(7*5)+(6*3)+(5*8)+(4*0)+(3*3)+(2*9)+(1*8)=128
128 % 10 = 8
So 53803-98-8 is a valid CAS Registry Number.

53803-98-8Downstream Products

53803-98-8Relevant academic research and scientific papers

Sulfonylation of C(sp3)–H bond for synthesis of 2-sulfolmethyl azaarenes catalyzed by TBAI in water

Dong, Dao-Qing,Gao, Xing,Li, Li-Xia,Hao, Shuang-Hong,Wang, Zu-Li

, p. 7557 - 7567 (2018)

A tetrabutylammonium iodide (TBAI)-catalyzed method for synthesis of 2-sulfolmethyl quinolone has been developed. Using water as solvent, a wide range of 2-sulfolmethyl quinolones were obtained in high to excellent yield. In addition, water and TBAI could be reused for five times without significant decrease of the yield of the corresponding product.

VICARIOUS SUBSTITUTION OF HYDROGEN IN AROMATIC HETEROCYCLES WITH CARBANIONS OF CHLOROMETHYL SULFONYL COMPOUNDS

Makosza, M.,Golinski, J.,Rykowski, A.

, p. 3277 - 3278 (2007/10/02)

Carbanions of chloromethyl phenylsulfone and chloromethane sulfonmorpholide replace hydrogen in benzothiazole, acridine and variety of substituted 1,2,4-triazines giving corresponding sulfonyl methylderivatives.

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