33856-07-4

Basic information

• Product Name: 3?(2?((4?methoxyphenyl)amino)thiazol?4?yl)?2H?chromen?2?one
• Synonyms: 3?(2?((4?methoxyphenyl)amino)thiazol?4?yl)?2H?chromen?2?one
• CAS NO: 33856-07-4
• Molecular Weight: 350.398
• Mol File: 33856-07-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3?(2?((4?methoxyphenyl)amino)thiazol?4?yl)?2H?chromen?2?one(CAS DataBase Reference)
• NIST Chemistry Reference: 3?(2?((4?methoxyphenyl)amino)thiazol?4?yl)?2H?chromen?2?one(33856-07-4)
• EPA Substance Registry System: 3?(2?((4?methoxyphenyl)amino)thiazol?4?yl)?2H?chromen?2?one(33856-07-4)

Safety Data

• Hazardous Substances Data: 33856-07-4(Hazardous Substances Data)

Upstream product

• 2293-07-4 1-(4-methoxyphenyl)thiourea 
• 90-02-8 salicylaldehyde 
• 2290-65-5 trimethylsilyl isothiocyanate 
• 29310-88-1 3-bromoacetylcoumarin 
• 104-94-9 4-methoxy-aniline 
• 3949-36-8 3-acetylcoumarin 
• 141099-74-3 3-(2-thiocyanatoacetyl)-2H-1-benzopyran-2-one 

Downstream Products

• 33856-15-4 5-Brom-4-(3'-cumarinyl)-2-p-methoxyphenylaminothiazol 

Relevant articles and documents

A Facile One-Step Multi-Component Approach toward the Synthesis of 3-(2-Amino-4-Thiazolyl)Coumarins by using Trimethylsilyl Isothiocyanate and their Antioxidant and Anti-Inflammatory Activity

A multi-component synthesis of 3-(2-amino-4-thiazolyl)coumarins has been reported from 3-(2-bromoacetyl)-2H-chromen-2-ones primary amines and using commercially available trimethylsilyl isothiocyanate. The structures of newly synthesized compounds were ch

PEG-600 mediated one-pot reaction of 3-acetyl-2: H -chromen-2-one with heterylthiols and phenylthioureas using tetrabutylammonium tribromide as an efficient green reagent

A simple method for the one-pot reaction of 3-acetyl-2H-chromen-2-one with different heterylthiols and phenylthioureas under green conditions using tetrabutylammonium tribromide (TBATB) as an efficient reagent has been described. 3-Acetyl-2H-chromen-2-one