Welcome to LookChem.com Sign In|Join Free
  • or
4-Chloro-N-(2-hydroxypropyl)benzenesulfonamide is a chemical compound with the molecular formula C9H12ClNO3S. It is a sulfonamide derivative that exhibits drug-like properties, making it a potential candidate for drug development. 4-Chloro-N-(2-hydroxypropyl)benzenesulfonaMide is synthesized through the reaction of 4-chloroaniline with chloroacetyl chloride, followed by treatment with sodium hydroxide and 2-hydroxypropylamine.

74668-38-5

Post Buying Request

74668-38-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

74668-38-5 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-N-(2-hydroxypropyl)benzenesulfonamide is used as a key intermediate in the synthesis of pharmaceutical compounds. Its drug-like properties and potential anti-inflammatory and anti-cancer activities make it a promising candidate for the development of new therapeutic agents.
Used in Drug Development:
4-Chloro-N-(2-hydroxypropyl)benzenesulfonamide is used as a potential therapeutic agent for anti-inflammatory and anti-cancer treatments. Its drug-like properties and potential therapeutic applications make it a valuable compound for further research and development in the pharmaceutical field.

Check Digit Verification of cas no

The CAS Registry Mumber 74668-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,6 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74668-38:
(7*7)+(6*4)+(5*6)+(4*6)+(3*8)+(2*3)+(1*8)=165
165 % 10 = 5
So 74668-38-5 is a valid CAS Registry Number.

74668-38-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-N-(2-hydroxypropyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-(2-Hydroxy-1,1-dimethylethyl)-2-(isopropyl)-5-methylcyclohexanecarboxamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74668-38-5 SDS

74668-38-5Downstream Products

74668-38-5Relevant 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).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 74668-38-5