33933-82-3 Usage
Uses
Used in the Food and Beverage Industry:
2-Decanone, 5,9-dimethylis used as a fragrance and flavoring agent for its distinctive sweet, fruity scent and taste, enhancing the sensory experience of various food and beverage products.
Used in the Coatings and Paints Industry:
As a solvent, 2-Decanone, 5,9-dimethylis utilized in the production of varnishes, paints, and coatings, contributing to the solubility and performance of these products by aiding in the application process and drying time.
Used in Chemical Synthesis:
2-Decanone, 5,9-dimethylserves as a chemical intermediate in the synthesis of other compounds, playing a crucial role in the creation of various chemical products through its reactivity and functional groups.
Safety Considerations:
It is essential to handle 2-Decanone, 5,9-dimethylwith care due to its potential harmful effects if inhaled or ingested, and its irritating properties to the skin and eyes. Adhering to safety protocols is imperative to minimize exposure and prevent health hazards in occupational settings.
Check Digit Verification of cas no
The CAS Registry Mumber 33933-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,3 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33933-82:
(7*3)+(6*3)+(5*9)+(4*3)+(3*3)+(2*8)+(1*2)=123
123 % 10 = 3
So 33933-82-3 is a valid CAS Registry Number.
33933-82-3Relevant academic research and scientific papers
Discovery of Lipophilic Bisphosphonates That Target Bacterial Cell Wall and Quinone Biosynthesis
Malwal, Satish R.,Chen, Lu,Hicks, Hunter,Qu, Fiona,Liu, Weidong,Shillo, Alli,Law, Wen Xuan,Zhang, Jianan,Chandnani, Neal,Han, Xu,Zheng, Yingying,Chen, Chun-Chi,Guo, Rey-Ting,Abdelkhalek, Ahmed,Seleem, Mohamed N.,Oldfield, Eric
supporting information, p. 2564 - 2581 (2019/03/07)
We report that alkyl-substituted bisphosphonates have activity against Bacillus anthracis Sterne (0.40 μg/mL), Mycobacterium smegmatis (1.4 μg/mL), Bacillus subtilis (1.0 μg/mL), and Staphylococcus aureus (13 μg/mL). In many cases, there is no effect of serum binding, as well as low activity against a human embryonic kidney cell line. Targeting of isoprenoid biosynthesis is involved with 74 having IC50 values of ～100 nM against heptaprenyl diphosphate synthase and 200 nM against farnesyl diphosphate synthase. B. subtilis growth inhibition was rescued by addition of farnesyl diphosphate, menaquinone-4 (MK-4), or undecaprenyl phosphate (UP), and the combination of MK-4 and UP resulted in a 25× increase in ED50, indicating targeting of both quinone and cell wall biosynthesis. Clostridioides difficile was inhibited by 74, and since this organism does not synthesize quinones, cell wall biosynthesis is the likely target. We also solved three X-ray structures of inhibitors bound to octaprenyl diphosphate and/or undecaprenyl diphosphate synthases.
