88227-04-7 Usage
Uses
Used in Pharmaceutical Industry:
(Z)-3-Methylhepta-2,6-dienoic acid is used as a synthetic intermediate for the production of various pharmaceuticals and natural products. Its unique structure allows for the synthesis of complex organic molecules, making it a valuable component in the development of new drugs and therapeutic agents.
Used in Flavors and Fragrances Industry:
(Z)-3-Methylhepta-2,6-dienoic acid is used as a starting material in the production of flavors and fragrances. Its potential use in creating unique scents and tastes makes it an important molecule in the development of new products in this industry.
Used in Pest Control Industry:
(Z)-3-Methylhepta-2,6-dienoic acid has been investigated for its insecticidal properties, making it of interest in the development of new pest control agents. Its potential to act as an effective insecticide could lead to the creation of innovative and environmentally friendly pest management solutions.
Overall, (Z)-3-Methylhepta-2,6-dienoic acid plays a crucial role in various chemical and biological applications, making it an important molecule in the field of science and industry. Its versatility and unique properties contribute to its wide range of uses across different industries, highlighting its significance in modern research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 88227-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,2 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88227-04:
(7*8)+(6*8)+(5*2)+(4*2)+(3*7)+(2*0)+(1*4)=147
147 % 10 = 7
So 88227-04-7 is a valid CAS Registry Number.
88227-04-7Relevant academic research and scientific papers
Examination of the olefin-olefin ring closing metathesis to prepare Latrunculin B
She, Jin,Lampe, John W.,Polianski, Alexandra B.,Watson, Paul S.
supporting information; experimental part, p. 298 - 301 (2009/04/14)
Three subunits of the potent actin polymerization inhibitor Latrunculin B were synthesized and assembled using olefin-olefin ring closing metathesis chemistry to close the 14-membered macrocycle. Metathesis reactions of substrates with various remote protecting group patterns were examined and gave 6,7-E-lactones as the preferred products.
Cytoskeletal active compounds, compositions and use
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Page/Page column 24, (2010/11/23)
The present invention is directed to synthetic cytoskeletal active compounds that are related to natural Latrunculin A or Latrunculin B. The present invention is also directed to pharmaceutical compositions comprising such compounds and a pharmaceutically
