146955-45-5 Usage
Uses
Used in Fragrance Industry:
(Z)-7-Tetradecen-2-one is used as a fragrance ingredient for its sweet, citrus-like aroma, adding a pleasant scent to various products.
Used in Pharmaceutical Industry:
(Z)-7-Tetradecen-2-one is used as a pharmaceutical compound due to its unique chemical properties, potentially contributing to the development of new medications.
Used in Agrochemical Industry:
(Z)-7-Tetradecen-2-one is used as an agrochemical compound for its insecticidal and fungicidal properties, making it a potential candidate for the development of eco-friendly pesticides and repellents.
Used in Eco-friendly Pesticides and Repellents Development:
(Z)-7-Tetradecen-2-one is used as an active ingredient in the development of eco-friendly pesticides and repellents, leveraging its insecticidal and fungicidal properties to provide effective pest control while minimizing environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 146955-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,5 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 146955-45:
(8*1)+(7*4)+(6*6)+(5*9)+(4*5)+(3*5)+(2*4)+(1*5)=165
165 % 10 = 5
So 146955-45-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O/c1-3-4-5-6-7-8-9-10-11-12-13-14(2)15/h8-9H,3-7,10-13H2,1-2H3/b9-8-
146955-45-5Relevant articles and documents
Design, synthesis and antimycobacterial activities of 1-methyl-2-alkenyl- 4(1H)-quinolones
Wube, Abraham A.,Hüfner, Antje,Thomaschitz, Christina,Blunder, Martina,Kollroser, Manfred,Bauer, Rudolf,Bucar, Franz
, p. 567 - 579 (2011/03/17)
A series of 23 new 1-methyl-2-alkenyl-4(1H)quinolones have been synthesized and evaluated in vitro for their antimycobacterial activities against fast growing species of mycobacteria, such as Mycobacterium fortuitum, M. smegmatis and M. phlei. The compounds displayed good to excellent inhibition of the growth of the mycobacterial test strains with improved antimycobacterial activity compared to the hit compound, evocarpine. The most active compounds, which possessed chain length of 11-13 carbons at position-2 displayed potent inhibitory effects with an MIC value of 1.0 mg/L. In a human diploid embryonic lung cell line, MRC-5 cytotoxicity assay, the alkaloids showed weak to moderate cytotoxic activity. Biological evaluation of these evocarpine analogues on the less pathogenic fast growing strains of mycobacteria showed an interesting antimycobacterial profile and provided significant insight into the structure-activity relationships.
