3220-60-8 Usage
Uses
Used in Biodiesel Production:
Methyl sterculate is used as a key component in the production of biodiesel, an alternative fuel source. Its high cetane number, low pour point, and good oxidative stability contribute to the efficiency and performance of biodiesel, making it a suitable candidate for this application.
Used in Antimicrobial Applications:
Methyl sterculate has demonstrated potential as an antimicrobial agent, suggesting its use in applications where the control of microbial growth is necessary. Further research is needed to determine its effectiveness and optimal use in this field.
Used in Antiviral Applications:
Similarly, methyl sterculate has shown promise as an antiviral agent, indicating its potential use in applications targeting the control and prevention of viral infections. Additional studies are required to fully understand its antiviral properties and establish its role in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 3220-60-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3220-60:
(6*3)+(5*2)+(4*2)+(3*0)+(2*6)+(1*0)=48
48 % 10 = 8
So 3220-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H36O2/c1-3-4-5-6-8-11-14-18-17-19(18)15-12-9-7-10-13-16-20(21)22-2/h3-17H2,1-2H3
3220-60-8Relevant academic research and scientific papers
A New Approach to Cyclopropene Fatty Acids involving 1,2-Deiodination
Baird, Mark S.,Grehan, Brendan
, p. 1547 - 1548 (2007/10/02)
Methyl sterculate and methyl α-hydroxysterculate have been prepared by deiodination of 1,2-diiodocyclopropanes with butyllithium at low temperature.
A new approach to cyclopropene fatty acids
Baird, Mark S.,Dale, Cynthia M.,Lytollis, William,Simpson, Michael J.
, p. 1521 - 1522 (2007/10/02)
A series of esters of cyclopropene fatty acids, including sterculic, malvalic and sterculynic acids, has been prepared by alkylation of the corresponding 1-lithiocyclopropenes.
