104514-85-4 Usage
Properties and specific content of 2(3H)-Thiazolone, 4-(1-methylethyl)-
A chemical compound consisting of six carbon atoms, nine hydrogen atoms, one nitrogen atom, one oxygen atom, and one sulfur atom.
Thiazolone derivative
A heterocyclic compound containing a thiazolone ring (a five-membered ring with one sulfur and one oxygen atom).
Methyl group attachment
A methyl group (CH3) is attached to the carbon atom at position four of the thiazolone ring, affecting the compound's properties and reactivity.
Heterocyclic compounds
Contains atoms of different elements (heteroatoms) within its ring structure, contributing to its wide-ranging biological activities.
Biological activities
Thiazolones have been found to exhibit various biological activities, making them important in the development of pharmaceuticals and agrochemicals.
Potential therapeutic applications
The 4-(1-methylethyl)substitution on the thiazolone ring may provide specific properties that could be useful in medicinal chemistry and drug discovery.
Valuable building block
2(3H)-Thiazolone, 4-(1-methylethyl)may serve as a starting point for the synthesis of novel compounds with diverse biological activities, further expanding its potential applications in the field of chemistry and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 104514-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,1 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104514-85:
(8*1)+(7*0)+(6*4)+(5*5)+(4*1)+(3*4)+(2*8)+(1*5)=94
94 % 10 = 4
So 104514-85-4 is a valid CAS Registry Number.
104514-85-4Relevant academic research and scientific papers
Synthesis of Thiazolidinones from 1,4-Dithiocyanatobut-2-enes and their Use as Masked 2-Amino-1-mercaptobut-3-enes
Elall, Eatedal H. M. Abd,Ashmawy, Mohamed I. Al,Mellor, John M.
, p. 2729 - 2736 (2007/10/02)
1,4-Dithiocyanatobut-2-enes can be readily prepared from either the appropriate buta-1,3-diene or 1,4-dihalogenobut-2-ene, and give, on heating in methanol, thiazolidinones via -sigmatropic rearrangement.The initial products of this rearrangement, vi
