77627-63-5

Basic information

• Product Name: Ethanol, 2-[(4-phenyl-2-thiazolyl)amino]-
• CAS NO: 77627-63-5
• Molecular Formula: C11H12N2OS
• Molecular Weight: 220.295
• Mol File: 77627-63-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanol, 2-[(4-phenyl-2-thiazolyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanol, 2-[(4-phenyl-2-thiazolyl)amino]-(77627-63-5)
• EPA Substance Registry System: Ethanol, 2-[(4-phenyl-2-thiazolyl)amino]-(77627-63-5)

Safety Data

• Hazardous Substances Data: 77627-63-5(Hazardous Substances Data)

Upstream product

• 333-20-0 potassium thioacyanate 
• 54300-24-2 (2-hydroxy-ethyl)ammonium acetate 
• 70-11-1 α-bromoacetophenone 
• 29146-81-4 β-Hydroxyethylthiourea 
• 141-43-5 ethanolamine 
• 1826-23-9 2-chloro-4-phenylthiazole 

Downstream Products

• 77627-65-7 N-<2-(4'-phenylthiazol-2'-ylamino)ethyl>-N'-(o-tolyl)piperazine 
• 77627-66-8 N-<2-(4'-phenylthiazol-2'-ylamino)ethyl>-N'-phenylpiperazine 
• 113019-85-5 2--5-(1,3-dioxolidin-2-yl)-4-phenylthiazole 
• 113019-86-6 2--4-phenylthiazole-5-carbaldehyde-oxime 
• 113019-88-8 Acetic acid 2-[acetyl-(5-cyano-4-phenyl-thiazol-2-yl)-amino]-ethyl ester 
• 113019-83-3 2--4-phenylthiazole-5-carbaldehyde 
• 113019-87-7 2-(2-Acetoxyethylamino)-4-phenylthiazole-5-carbaldehyde-oxime 
• 113019-90-2 2-(2-Hydroxyethylamino)-4-phenylthiazole-5-carboxamidoxime 
• 113019-89-9 2-(2-Hydroxyethylamino)-4-phenylthiazole-5-carbonitrile 
• 113019-84-4 2-(2-Hydroxyethylamino)-4-phenylthiazole-5-carbaldehyde 
• 77627-64-6 2-N-(β-chloroethylamino)-4-phenylthiazole 
• 113019-82-2 Acetic acid 2-[acetyl-(4-phenyl-thiazol-2-yl)-amino]-ethyl ester 

Relevant articles and documents

One pot synthesis using supported reagents system KSCN/SiO 2-RNH3OAc/Al2O3: Synthesis of 2-aminothiazoles and N-allylthioureas

A simple and efficient method has been developed for the synthesis of 2-aminothiazoles and N-allylthioureas from commercially available materials in one pot by using a supported reagents system, KSCN/SiO2-RNH 3OAc/Al2O3, in which α-halo ketone reacts first KSCN/SiO2 and the product, α-thiocyanatoketone, reacts with RNH3OAc/Al2O3 to give the final product, 2-aminothiazoles, in good yield and allyl bromide reacts with KSCN/SiO 2 and the product, allyl isothiocyanate, reacts with RNH 3OAc/Al2O3 to give N-allylthiourea.

Synthesis of N-(2-Substituted-ethyl)-N'-arylpiperazines and Their Quaternary Salts as Potential Antihookworm Agents

A series of N-(2-substituted-ethyl)-N'-arylpiperazines (4-15) and their quaternary salts (17-21) have been prepared and tested for their antihookworm activity against Nippostrongylus brasiliensis in rats and Nematospiroides dubius in mice.Of the compounds