383-48-2 Usage
Description
N-Ethyl 4-fluorobenzenesulfonamide is a chemical compound with the molecular formula C8H10FNO2S. It is derived from benzenesulfonamide, featuring an ethyl group attached to the nitrogen atom and a fluorine atom on the benzene ring. N-Ethyl 4-fluorobenzenesulfonamide is known for its ability to inhibit the activity of certain enzymes, making it a valuable intermediate in the synthesis of pharmaceuticals and other organic compounds.
Uses
Used in Pharmaceutical Industry:
N-Ethyl 4-fluorobenzenesulfonamide is used as an intermediate in the synthesis of pharmaceuticals for its enzyme-inhibiting properties. It plays a crucial role in drug development and research, contributing to the creation of new medications with potential therapeutic applications.
Used in Chemical Industry:
As a versatile chemical intermediate, N-Ethyl 4-fluorobenzenesulfonamide is used in the synthesis of various organic compounds, making it an important building block in the production of a wide range of chemical products.
Used in Agricultural Industry:
N-Ethyl 4-fluorobenzenesulfonamide may have potential applications as a pesticide or herbicide due to its chemical properties. Its ability to inhibit enzyme activity could be harnessed to control or eliminate unwanted plant or insect species, contributing to more effective and targeted agricultural solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 383-48-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 383-48:
(5*3)+(4*8)+(3*3)+(2*4)+(1*8)=72
72 % 10 = 2
So 383-48-2 is a valid CAS Registry Number.
383-48-2Relevant articles and documents
Chromoselective Synthesis of Sulfonyl Chlorides and Sulfonamides with Potassium Poly(heptazine imide) Photocatalyst
Antonietti, Markus,Guldi, Dirk M.,Markushyna, Yevheniia,Savateev, Aleksandr,Schü?lbauer, Christoph M.,Ullrich, Tobias
supporting information, p. 20543 - 20550 (2021/08/12)
Among external stimuli used to promote a chemical reaction, photocatalysis possesses a unique one—light. Photons are traceless reagents that provide an exclusive opportunity to alter chemoselectivity of the photocatalytic reaction varying the color of incident light. This strategy may be implemented by using a sensitizer capable to activate a specific reaction pathway depending on the excitation light. Herein, we use potassium poly(heptazine imide) (K-PHI), a type of carbon nitride, to generate selectively three different products from S-arylthioacetates simply varying the excitation light and otherwise identical conditions. Namely, arylchlorides are produced under UV/purple, sulfonyl chlorides with blue/white, and diaryldisulfides at green to red light. A combination of the negatively charged polyanion, highly positive potential of the valence band, presence of intraband states, ability to sensitize singlet oxygen, and multi-electron transfer is shown to enable this chromoselective conversion of thioacetates.
