294659-11-3 Usage
Uses
Used in Organic Synthesis:
(E)-methyl 10-nitrooctadec-9-enoate is used as a precursor in the synthesis of other organic compounds for various applications, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure with a nitro group and a double bond allows for further functionalization and modification in organic synthesis.
Used in Chemical Intermediates:
In the chemical industry, (E)-methyl 10-nitrooctadec-9-enoate is used as a chemical intermediate, which is a substance that is produced and used specifically for the purpose of being converted into another compound. Its role as an intermediate is crucial in the production of more complex and valuable chemicals.
Used in Research and Development:
(E)-methyl 10-nitrooctadec-9-enoate is also utilized in research and development in the field of organic chemistry. Its unique properties and reactivity make it an interesting compound for scientists to study and explore its potential applications and reactions.
Potential Pharmaceutical or Biological Activity:
While not explicitly mentioned in the provided materials, (E)-methyl 10-nitrooctadec-9-enoate may have potential pharmaceutical or biological activity. However, more research is needed to fully understand its properties and potential uses in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 294659-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,6,5 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 294659-11:
(8*2)+(7*9)+(6*4)+(5*6)+(4*5)+(3*9)+(2*1)+(1*1)=183
183 % 10 = 3
So 294659-11-3 is a valid CAS Registry Number.
294659-11-3Relevant academic research and scientific papers
Dietz, Ulrich,Frank, Andrea,Lehr, Alexander,Münch, Winfried,Nubbemeyer, Udo
, p. 3295 - 3304 (2019)
Extensive investigation of nitrated phospholipids in connection with various biologically important processes requires reliable access to suitable material. A selective chemical synthesis introducing a defined nitrofatty acid at the sn -2 position of a 2-lyso sn -glycero-3-phosphatidylcholine was developed. Given that the nitroalkene moiety of both reactant nitrofatty acid derivative and the product esters is characterised by particular sensitivity to nucleophile addition and, depending on the intermediate, subsequent olefin isomerisation and retro-Henry-type reaction, a reliable two-step ester formation was introduced. The activation of the nitrofatty acid succeeded after reaction with trichlorobenzoyl chloride, and the mixed anhydride could be isolated via extractive work-up. Subsequent reaction with 1-palmitoyl-2-lyso- sn -glycero-3-phosphatidylcholine enabled the sn -2 esterification to be achieved with high yield by using a minimum of reagents, avoiding the formation of side products and facilitating final isolation and purification.
