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9-ethyl-9H-carbazole-3-sulfonyl chloride is a chemical compound with the molecular formula C16H14ClNO2S. It is an organosulfur compound and belongs to the class of carbazole derivatives. 9-ethyl-9H-carbazole-3-sulfonyl chloride is characterized by its strong electrophilic properties due to the sulfonyl chloride group, making it a versatile and valuable intermediate in organic chemistry. Its unique chemical properties have led to its widespread utilization in the research and development of new materials and compounds across various industries.

24525-01-7

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24525-01-7 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
9-ethyl-9H-carbazole-3-sulfonyl chloride is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its ability to introduce carbazole moieties into different organic molecules makes it a valuable component in the development of new drugs and pesticides.
Used in Organic Synthesis:
As a reagent in organic synthesis, 9-ethyl-9H-carbazole-3-sulfonyl chloride is used to introduce carbazole moieties into different organic molecules. Its strong electrophilic properties allow for efficient reactions, contributing to the synthesis of a wide range of organic compounds.
Used in Research and Development:
Due to its unique chemical properties, 9-ethyl-9H-carbazole-3-sulfonyl chloride is widely utilized in the research and development of new materials and compounds in various industries. Its versatility as an intermediate enables the exploration of novel applications and advancements in chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 24525-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,2 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24525-01:
(7*2)+(6*4)+(5*5)+(4*2)+(3*5)+(2*0)+(1*1)=87
87 % 10 = 7
So 24525-01-7 is a valid CAS Registry Number.

24525-01-7Relevant academic research and scientific papers

Synthesis and spectral studies of 2-[(N-ethyl carbazole)-3-sulfonyl ethylenediamine]-1-N,N-2-(2-methypyridy) as a fluorescence probe for Zn 2+

Zhang, Jun,Cui, Huiling,Hojo, Masashi,Shuang, Shaomin,Dong, Chuan

, p. 343 - 346 (2012/03/11)

A novel Zn2+ fluorescence probe, 2-[(N-ethyl carbazole)-3-sulfonyl ethylenediamine]-1-N,N-bis(2-methypyrbidy), was designed and synthesized via simple steps, and its structure was confirmed by IR and 1H NMR. The probe gives significant fluorescence enhancement immediately following Zn2+ addition at neutral pH and exhibits improved selectivity for Zn2+ compared to the other metal ions in aqueous solution. The spectra and fluorescence quantum yield of the synthesized compound were carefully investigated by UV-vis absorption and fluorescence spectra in various solvents.

Novel pyridinyl and pyrimidinylcarbazole sulfonamides as antiproliferative agents

Hu, Laixing,Li, Zhuo-rong,Wang, Yue-ming,Wu, Yanbin,Jiang, Jian-Dong,Boykin, David W.

, p. 1193 - 1196 (2008/01/27)

A series of azaheterocyclic carbazole sulfonamides was synthesized and evaluated for antiproliferative activity. The most potent compounds N-(2,6-dimethoxypyridine-3-yl)-9-ethyl and 9-methylcarbazole-3-sulfonamide (13 and 14) gave significant cytotoxicity (IC50 = 122 and 101 nM). Compound 13 displayed submicromolar activities against seven human tumor cell lines. The SARs of this series of sulfonamides which includes the influence of azaheterocycle rings, sulfonamide linkage, and the carbazole ring are described.

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