56799-95-2 Usage
Description
4-Chloro-N-(1-naphthyl)benzenesulfonaMide, 97% is a chemical compound with the molecular formula C16H12ClNO2S. It is a white to off-white powder with a purity of 97%. 4-Chloro-N-(1-naphthyl)benzenesulfonaMide, 97% is commonly used as a reagent in organic synthesis and as a building block in the production of pharmaceuticals, dyes, and agrochemicals. It is also utilized in the manufacturing of polymers, and as an intermediate in the synthesis of various chemical compounds. It is important to handle this compound with care, as it may pose certain health and environmental hazards, and proper safety measures should be followed when handling and storing this substance.
Uses
Used in Pharmaceutical Industry:
4-Chloro-N-(1-naphthyl)benzenesulfonaMide, 97% is used as a building block for the production of pharmaceuticals. It plays a crucial role in the synthesis of various drug molecules, contributing to the development of new medications.
Used in Dye Industry:
In the dye industry, 4-Chloro-N-(1-naphthyl)benzenesulfonaMide, 97% is used as a building block for the production of dyes. Its unique chemical structure allows for the creation of a wide range of colors and properties in dye formulations.
Used in Agrochemical Industry:
4-Chloro-N-(1-naphthyl)benzenesulfonaMide, 97% is used as a building block in the production of agrochemicals. It contributes to the development of effective pesticides, herbicides, and other agricultural chemicals that help protect crops and enhance agricultural productivity.
Used in Polymer Industry:
In the polymer industry, 4-Chloro-N-(1-naphthyl)benzenesulfonaMide, 97% is used in the manufacturing of polymers. Its incorporation into polymer structures can enhance properties such as strength, durability, and resistance to environmental factors.
Used as a Reagent in Organic Synthesis:
4-Chloro-N-(1-naphthyl)benzenesulfonaMide, 97% is used as a reagent in organic synthesis. It serves as an intermediate in the synthesis of various chemical compounds, enabling the production of a wide range of products across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 56799-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,9 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56799-95:
(7*5)+(6*6)+(5*7)+(4*9)+(3*9)+(2*9)+(1*5)=192
192 % 10 = 2
So 56799-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H12ClNO2S/c17-13-8-10-14(11-9-13)21(19,20)18-16-7-3-5-12-4-1-2-6-15(12)16/h1-11,18H
56799-95-2Relevant articles and documents
Iridium-catalyzed reaction of 1-naphthols, N-(1-naphthyl)benzenesulfonamides, and salicylaldehyde with internal alkynes
Nishinaka, Yuko,Satoh, Tetsuya,Miura, Masahiro,Morisaka, Hideaki,Nomura, Masakatsu,Matsui, Hisaji,Yamaguchi, Chiharu
, p. 1727 - 1735 (2007/10/03)
1-Naphthols efficiently couple with internal alkynes via cleavage of the C-H bond at the peri-position in the presence of a catalyst system of [IrCl(cod)]2/PBut′3 to selectively afford the corresponding 8-vinyl-1-naphthol derivatives. N-(1-Naphthyl)benzenesulfonamides can similarly react with the alkynes. The reaction of salicylaldehyde with the alkynes using the catalyst system gives 2-hydroxyphenyl vinyl ketones via cleavage of the aldehyde C-H bond.
