13343-95-8 Usage
Description
1-(2-furyl)-3-(2-thienyl)-2-propen-1-one, with the molecular formula C11H8OS, is a yellow crystalline chemical compound characterized by a strong odor. It features a unique structure with a furan ring and a thiophene ring attached to a propenyl group, which contributes to its diverse applications.
Uses
Used in Flavor and Fragrance Industry:
1-(2-furyl)-3-(2-thienyl)-2-propen-1-one is used as a key compound for the production of flavors and fragrances due to its distinct and strong odor. Its unique chemical structure allows it to contribute to a wide range of scents and tastes in various consumer products.
Used in Pharmaceutical Development:
1-(2-furyl)-3-(2-thienyl)-2-propen-1-one is used as an active ingredient in the development of pharmaceuticals, particularly for its antibacterial and antifungal properties. These characteristics make it a promising candidate for creating new drugs to combat various infections and diseases.
Used in Antimicrobial Agents:
1-(2-furyl)-3-(2-thienyl)-2-propen-1-one is used as an antimicrobial agent for its ability to inhibit the growth of bacteria and fungi. Its application in this field can be beneficial in creating new products to maintain hygiene and prevent the spread of infections.
Used as a Food Preservative:
1-(2-furyl)-3-(2-thienyl)-2-propen-1-one is studied for its potential use as a food preservative, capitalizing on its antimicrobial properties to extend the shelf life of various food products and reduce the risk of spoilage and contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 13343-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,4 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13343-95:
(7*1)+(6*3)+(5*3)+(4*4)+(3*3)+(2*9)+(1*5)=88
88 % 10 = 8
So 13343-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O2S/c12-10(11-4-1-7-13-11)6-5-9-3-2-8-14-9/h1-8H/b6-5+
13343-95-8Relevant articles and documents
Synthesis, molecular docking and antimicrobial activity of new fused pyrimidine and pyridine derivatives
Radwan, Mohamed A.A.,Alshubramy, Maha A.,Abdel-Motaal, Marwa,Hemdan, Bahaa A.,El-Kady, Dina S.
, (2020)
Synthesis of some new heterocyclic ring systems incorporated pyrimidine and pyridine moieties starting from 1-(furan-2-yl)-3-(thiophen-2-yl) chalcone was achieved. The structure of the new compounds was interpreted by spectral studies and ESI-MS analysis.
Synthesis, cyclooxygenase inhibition, anti-inflammatory evaluation, and ulcerogenic liability of new 1,3,5-triarylpyrazoline derivatives possessing a methanesulfonyl pharmacophore
Abdellatif, Khaled R. A.,Fadaly, Wael A. A.,Azouz, Amany A.
, p. 1 - 7 (2016/10/11)
A new series of 1,3,5-triarylpyrazolines 13a–l was synthesized and all prepared compounds were evaluated for their in vitro COX-1/COX-2 inhibitory activity and in vivo anti-inflammatory activity. All test compounds were more selective for the COX-2 isozyme and showed good in vivo anti-inflammatory activity. Compound 13h was the most COX-2 selective compound (COX-2 selectivity index (SI)=10.23) and the most potent anti-inflammatory derivative (ED50-60.1μmol/kg) in comparison with celecoxib (COX-2 SI=9.29 and ED50=81.4μmol/kg). All screened compounds were less ulcerogenic (ulcer indexes (UI)=0.33–1.33) than aspirin (UI=2.33) and comparable to celecoxib (UI=0.33).
Atom-efficient, solvent-free, green synthesis of chalcones by grinding
Rateb, Nora M.,Zohdi, Hussein F.
experimental part, p. 2789 - 2794 (2009/12/06)
An improved Claisen-Schmidt condensation reaction of methyl ketones and aromatic aldehydes can be achieved by grinding at room temperature in the absence of solvents. This process is simple, efficient, economical, and environmentally benign compared to classical reactions.
