5744-31-0

Basic information

• Product Name: 4,5-dihydro-4,4-dimethyl-N-phenyl-2-thiazolamine
• Synonyms: 4,5-dihydro-4,4-dimethyl-N-phenyl-2-thiazolamine
• CAS NO: 5744-31-0
• Molecular Weight: 206.312
• Mol File: 5744-31-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,5-dihydro-4,4-dimethyl-N-phenyl-2-thiazolamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-dihydro-4,4-dimethyl-N-phenyl-2-thiazolamine(5744-31-0)
• EPA Substance Registry System: 4,5-dihydro-4,4-dimethyl-N-phenyl-2-thiazolamine(5744-31-0)

Safety Data

• Hazardous Substances Data: 5744-31-0(Hazardous Substances Data)

Upstream product

• 2654-06-0 N-[(1,1-dimethyl-2-hydroxy)ethyl]-N'-phenylthiourea 
• 103-72-0 phenyl isothiocyanate 
• 927-82-2 2-amino-2-methylpropyl hydrogensulfate 

Relevant articles and documents

A Bench-Stable Vilsmeier Reagent for in situ Alcohol Activation: Synthetic Application in the Synthesis of 2-Amino-2-Thiazolines

A robust, chemoselective direct condensation/cyclization of thioureas and amino alcohols is described. Employing a bench-stable Vilsmeier reagent, methoxymethylene- N, N -dimethyliminium methyl sulfate, the selective in situ activation of alcohols is achieved with high efficiency and broad functional-group tolerance. The reversible interaction of the Vilsmeier reagent with substrate was key to the success of this activation strategy.

Development of Amino-Oxazoline and Amino-Thiazoline Organic Catalysts for the Ring-Opening Polymerisation of Lactide

The ring-opening polymerisation of lactide by a range of aminooxazoline and amino-thiazoline catalysts is reported. The more electronrich derivatives are demonstrated to be the most highly active and polymerisation is well controlled, as evidenced by the