2748-18-7 Usage
Type of compound
Heterocyclic compound
Structural features
a. Contains an imidazole ring
b. Contains a sulfanylcarbothioyl group
Functional groups
a. Imidazolium
b. Sulfanyl (-SH)
c. Carbothioyl (C=S)
Applications
a. Reagent in organic synthesis
b. Precursor in the production of pharmaceuticals and agrochemicals
Biological and pharmacological properties
a. Antimicrobial activity
b. Anticancer activity
Other potential uses
a. Materials science
b. Drug delivery
c. Medical imaging
Chemical structure
The compound consists of a 5-membered imidazole ring fused to a 4-membered dihydro ring. The 1 and 3 positions of the imidazole ring are substituted with ethyl groups, and the 2 position is substituted with a sulfanylcarbothioyl group.
Check Digit Verification of cas no
The CAS Registry Mumber 2748-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2748-18:
(6*2)+(5*7)+(4*4)+(3*8)+(2*1)+(1*8)=97
97 % 10 = 7
So 2748-18-7 is a valid CAS Registry Number.
2748-18-7Relevant academic research and scientific papers
Electron-rich Olefins, 6. - CS2 Dipoles from Elektron-rich Olefins - Synthesis and Cycloaddition Reactions
Krasuski, Witold,Nikolaus, Dieter,Regitz, Manfred
, p. 1451 - 1465 (2007/10/02)
The electron-rich olefins 1a-e and 7 react with carbon disulfide in a molar ration of 1:2 to yield the stable dipoles 5a-e and 8; in the case of 5f the imidazolidine 6 is the starting material.The dipoles are characterized by protonation with acetylenedic
