1287721-80-5

Basic information

• Product Name: C₂₃H₁₅ClN₄O₄S₂
• CAS NO: 1287721-80-5
• Molecular Weight: 510.981
• Mol File: 1287721-80-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₃H₁₅ClN₄O₄S₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₃H₁₅ClN₄O₄S₂(1287721-80-5)
• EPA Substance Registry System: C₂₃H₁₅ClN₄O₄S₂(1287721-80-5)

Safety Data

• Hazardous Substances Data: 1287721-80-5(Hazardous Substances Data)

Upstream product

• 14062-27-2 ethyl 4-methylthiophenylacetate 
• 16188-55-9 2-(4-(methylthio)phenyl)acetic acid 
• 1263796-97-9 3-(4-methylthiobenzyl)-1,2,4-triazole-5-thiol 
• 79-11-8 chloroacetic acid 
• 480439-09-6 5-(4-chloro-2-nitrophenyl)-2-furaldehyde 
• 1313870-47-1 4-methylthiophenylacetyl thiosemicarbazide 
• 1257393-74-0 (4-methylthiophenyl)acetic acid hydrazide 

Relevant articles and documents

Three-component reaction: Synthesis, characterization, and biological study of some fused bridgehead nitrogen heterocyclic systems containing 4-methylthiophenyl moiety

Several substituted thiazolo-[3,2-b]-1,2,4-triazole derivatives 4 were synthesized by a one-pot, three-component reaction of 3-(4-methylthiobenzyl)-1, 2,4-triazole-5-thiol 3, substituted 5-aryl-furan-2-carboxaldehydes/substituted aromatic aldehydes, and monochloroacetic acid in acetic acid using acetic anhydride and anhydrous sodium acetate. Compound 3 was obtained from 4-methylthiophenyl acetic acid by esterification followed by hydrazinolysis. All structures of the newly synthesized compounds were elucidated by elemental analysis and spectral data. The newly synthesized compounds were also screened for their antimicrobial and anti-inflammatory activities. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. Copyright Taylor & Francis Group, LLC.