915302-74-8 Usage
Uses
Used in Pharmaceutical Industry:
C36H43N5O5 is used as a potential therapeutic agent for various medical applications. Its complex structure and the presence of nitrogen and oxygen atoms indicate that it may have biological activity and could be involved in various physiological processes.
Used in Research and Development:
C36H43N5O5 serves as a subject of study in scientific research, particularly in the fields of organic chemistry, biochemistry, and molecular biology. Its structure and properties can provide insights into the design and synthesis of new compounds with potential applications in medicine, agriculture, and other industries.
Used in Drug Delivery Systems:
C36H43N5O5 can be utilized as a component in the development of drug delivery systems, where its complex structure and functional groups may contribute to the controlled release and targeted delivery of therapeutic agents.
Used in Cosmetics Industry:
C36H43N5O5 may be employed as an active ingredient in cosmetic products, where its complex structure and potential biological activity could offer benefits such as skin protection, anti-aging, or moisturizing effects.
Used in Agricultural Industry:
C36H43N5O5 could be used as a component in agricultural products, such as pesticides or fertilizers, where its complex structure and potential biological activity may contribute to the enhancement of crop yield or protection against pests and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 915302-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,3,0 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 915302-74:
(8*9)+(7*1)+(6*5)+(5*3)+(4*0)+(3*2)+(2*7)+(1*4)=148
148 % 10 = 8
So 915302-74-8 is a valid CAS Registry Number.
915302-74-8Relevant academic research and scientific papers
Discovery, synthesis, and insecticidal activity of cycloaspeptide E
Lewer, Paul,Graupner, Paul R.,Hahn, Donald R.,Karr, Laura L.,Duebelbeis, Dennis O.,Lira, Justin M.,Anzeveno, Peter B.,Fields, Stephen C.,Gilbert, Jeffrey R.,Pearce, Cedric
, p. 1506 - 1510 (2008/12/22)
Several Penicillia and one Tricothecium strain produced a new, insecticidally active member of the cycloaspeptide family, with the proposed name cycloaspeptide E (1). The structure, which was determined on the basis of spectroscopic (NMR, UV, MS) data and Marfey amino acid analysis, was the tyrosine desoxy version of cycloaspeptide A (2). Two synthetic routes to compound 1 were developed: one a partial synthesis from 2 and the other a total synthesis from methyl alaninate hydrochloride. Cycloaspeptide E, the first member of this series not to contain a tyrosine moiety, is also the first to be reported with insecticidal activity.
