6419-69-8 Usage
Uses
Used in Organic Synthesis:
4-Chloro-N-(2-Hydroxyethyl)benzenesulfonamide is used as a chemical intermediate for the production of a wide range of chemical products. Its role in organic synthesis is crucial, as it contributes to the creation of various compounds that have applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Chloro-N-(2-Hydroxyethyl)benzenesulfonamide is used as a building block for the synthesis of various drugs. Its versatility in organic synthesis allows for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Production:
4-Chloro-N-(2-Hydroxyethyl)benzenesulfonamide is used as a key component in the production of various chemical products. Its presence in the synthesis process is essential for creating a diverse array of chemical compounds that serve different purposes in various industries.
Used in Research and Development:
In the field of research and development, 4-Chloro-N-(2-Hydroxyethyl)benzenesulfonamide is used as a subject of study for understanding its properties, potential applications, and safety. This research can lead to the discovery of new uses and applications for the compound, as well as insights into its toxicity and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 6419-69-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6419-69:
(6*6)+(5*4)+(4*1)+(3*9)+(2*6)+(1*9)=108
108 % 10 = 8
So 6419-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClNO3S/c9-7-1-3-8(4-2-7)14(12,13)10-5-6-11/h1-4,10-11H,5-6H2
6419-69-8Relevant academic research and scientific papers
Chemistry of Sulfonyl Isocyanates and Sulfonyl Isothiocyanates. IX. Routes to Substituted Oxazolidin-2-ones and Oxazolidine-2-thiones
McFarland, J. W.,Hayes, C. E.,Blair, E. B.,Stuhlmacher, K. R.
, p. 271 - 272 (2007/10/02)
4-Chlorobenzenesulfonyl isocyanate (I) reacted with 2-chloroethanol and 1-chloro-2-propanol to give, respectively, 2-choroethyl-4-chlorobenzenesulfonyl carbamate (III) and 1-chloro-2-propyl-4-chlorobenzenesulfonyl carbamate (VI).The carbamates III and VI cyclized under the influence of pyridine to afford, respectively, 3-(4-chlorobenzenesulfonyl)oxazolidin-2-one (IV) and 3-(4-chlorobenzenesulfonyl)-5-methyloxazolidin-2-one (VII).The oxazolidin-2-ones were stable toward hydrochloric acid but hydrolyzed in 2M sodium hydroxide solution to N-(2-hydroxyethyl)-4-chlorobenzenesulfonamide (V) and N-(2-hydroxy-1-propyl)-4-chlorobenzenesulfonamide (VIII), respectively. 4-Toluenesulfonyl isothiocyanate (II) reacted with 2-chloroethanol to give 2-chloroethyl-4-chlorobenzenesulfonyl thiocarbamate (IX), which was converted by pyridine to 3-(4-toluenesulfonyl)oxazolidine-2-thione. (X).
