5316-74-5 Usage
Thiazole derivative
It is a compound that is derived from thiazole, a five-membered heterocyclic aromatic ring system.
Contains a phenyl group
A phenyl group is a group of atoms in a molecule that consists of a ring of six carbon atoms with a hydrogen atom attached to each carbon atom, it is a basic structural unit in many organic compounds.
Contains an ethylthio group
An ethylthio group is a group of atoms in a molecule that consists of an ethyl group (a two-carbon chain with a hydrogen atom attached to each carbon atom) bonded to a sulfur atom.
Used in organic synthesis and pharmaceutical research
2-(ethylthio)-4-phenylthiazole is used as a building block or reagent in the synthesis of other organic compounds, and in the development of new drugs.
Potential biological activities
2-(ethylthio)-4-phenylthiazole has been studied for its ability to inhibit the growth of microorganisms, fungi, and cancer cells.
Antimicrobial, antifungal, and anticancer properties
These are some of the potential biological activities that have been observed in 2-(ethylthio)-4-phenylthiazole, indicating its potential as a therapeutic agent.
Potential in the development of new drugs
2-(ethylthio)-4-phenylthiazole has been studied for its potential use in the development of new drugs due to its biological activities.
Chemical intermediate in the synthesis of other organic compounds
2-(ethylthio)-4-phenylthiazole is used as a building block or reagent in the synthesis of other organic compounds, indicating its versatility in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 5316-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5316-74:
(6*5)+(5*3)+(4*1)+(3*6)+(2*7)+(1*4)=85
85 % 10 = 5
So 5316-74-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NS2/c1-2-13-11-12-10(8-14-11)9-6-4-3-5-7-9/h3-8H,2H2,1H3
5316-74-5Relevant academic research and scientific papers
Reactions of 1-alkynyl thiocyanates with nucleophilic reagents. Synthesis of 2,4-disubstituted 1,3-thiazoles
Jong, R.L.P. de,Meijer, J.,Sukhai, R.S.,Bradsma, L.
, p. 310 - 313 (2007/10/02)
Reaction of 1-alkynyl thiocyanates RCC-S-CN (1) with alcohols, phenol or thiols or secondary aliphatic amines in the presence of anhydrous zinc chloride or boron trifluoride diethyl etherate gives mixtures of 2,4-disubstituted 1,3-thiazoles (2), thiocarbonyl compounds (3) (thiono esters, dithio esters or thioamides) and 2-alkylidene-1,3-dithioles (4).In all cases, the 1,3-thiazoles can be obtained in good yields if the proper reaction conditions are applied.Interaction between 1 and lithium dialkylamides LiNR'2 gives the compounds RCC-S-NR'2 (5) (attack on sulfur).With alkoxides R'O1-, the primary attack is on CN: the in termediacy alkynethiolate RCC-S1- subsequently reacts with the alkyl cyanate R'OCN to afford 1-alkynyl sulfides RCC-SR'(6)
