876694-43-8 Usage
Description
3-Bromo-N-cyclopropylbenzenesulphonamide 98, a sulphonamide derivative, is a chemical compound with a molecular formula of C8H9BrNO2S and a molecular weight of 263.13 g/mol. It is characterized by its versatile properties and potential applications in various industrial and research fields, making it an important compound in the realm of organic chemistry.
Uses
Used in Pharmaceutical Industry:
3-Bromo-N-cyclopropylbenzenesulphonamide 98 is used as a building block for the synthesis of pharmaceuticals. Its unique structure and functional groups contribute to the development of new drugs with improved therapeutic properties and efficacy.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-N-cyclopropylbenzenesulphonamide 98 serves as a key component in the synthesis of agrochemicals. Its incorporation into these compounds enhances their effectiveness in pest control and crop protection, contributing to increased agricultural productivity.
Used in Organic Synthesis:
3-Bromo-N-cyclopropylbenzenesulphonamide 98 is utilized as a reagent in various organic synthesis processes. Its presence facilitates specific chemical reactions, enabling the production of a wide range of organic compounds for diverse applications.
Used in Chemical Research:
As a substrate for chemical research, 3-Bromo-N-cyclopropylbenzenesulphonamide 98 plays a crucial role in advancing the understanding of chemical reactions and mechanisms. Its unique properties and reactivity provide valuable insights into the development of new chemical processes and methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 876694-43-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,6,9 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 876694-43:
(8*8)+(7*7)+(6*6)+(5*6)+(4*9)+(3*4)+(2*4)+(1*3)=238
238 % 10 = 8
So 876694-43-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10BrNO2S/c10-7-2-1-3-9(6-7)14(12,13)11-8-4-5-8/h1-3,6,8,11H,4-5H2
876694-43-8Relevant articles and documents
Diastereoselective Photoredox-Catalyzed [3 + 2] Cycloadditions of N-Sulfonyl Cyclopropylamines with Electron-Deficient Olefins
White, Dawn H.,Noble, Adam,Booker-Milburn, Kevin I.,Aggarwal, Varinder K.
supporting information, p. 3038 - 3042 (2021/05/04)
A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopropylamines and electron-deficient olefins is reported. The reactions proceed via the oxidation of a sulfonamide aza-anion by an organic photocatalyst to generate a nitrogen-centered radical. Strain-induced ring opening and intermolecular addition to the olefin generate an intermediate carbon-centered radical that is reduced to an anion prior to 5-exo cyclization. This enables a highly diastereoselective construction of trans-cyclopentanes possessing synthetically useful functional groups.
STK4 INHIBITORS FOR TREATMENT OF HEMATOLOGIC MALIGNANCIES
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Paragraph 00690, (2017/01/09)
The application relates to compounds of Formula (I'): which modulate the activity of a kinase (e.g., STK4), a pharmaceutical composition comprising the compound, and a method of treating or preventing a disease or disorder associated with the modulation of a kinase, such as STK4.
SUBSTITUTED PYRIMIDINYL AND PYRIDINYL-PYRROLOPYRIDINONES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS
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Page/Page column 60; 61, (2014/05/24)
The present invention relates to substituted pyrimidinyl- and pyridinylpyrrolopyridinone compounds which modulate the activity of protein kinases and are therefore useful in treating diseases caused by dysregulated protein kinase activity, in particular RET family kinases. The present invention also provides methods for preparing these compounds, pharmaceutical compositions comprising these compounds, and methods of treating diseases utilizing pharmaceutical compositions containing these compounds.