72849-42-4 Usage
Uses
Used in Polymer and Plastics Industry:
Heptadecanedioic acid, monomethyl ester is used as a component in the production of polymers and plastics for its ability to enhance the durability and flexibility of these materials.
Used in Lubricants Industry:
In the lubricants industry, heptadecanedioic acid, monomethyl ester serves as an additive to improve the performance and longevity of lubricating products, thanks to its high molecular weight and ability to reduce friction.
Used in Cosmetics and Personal Care Industry:
Heptadecanedioic acid, monomethyl ester is used as an ingredient in cosmetics and personal care products due to its potential antioxidant properties, which can help protect the products and the skin from oxidative stress.
Used in Pharmaceutical Industry:
Heptadecanedioic acid, monomethyl ester may be utilized in the pharmaceutical industry for drug delivery systems, taking advantage of its chemical properties to improve the efficacy and targeted delivery of pharmaceutical compounds.
Used as a Precursor in Synthesis:
In the synthesis of bioactive compounds, heptadecanedioic acid, monomethyl ester acts as a valuable precursor, contributing to the creation of new pharmaceuticals or other bioactive substances.
Check Digit Verification of cas no
The CAS Registry Mumber 72849-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,4 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72849-42:
(7*7)+(6*2)+(5*8)+(4*4)+(3*9)+(2*4)+(1*2)=154
154 % 10 = 4
So 72849-42-4 is a valid CAS Registry Number.
72849-42-4Relevant academic research and scientific papers
HETEROCYCLIC DERIVATIVES
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Page/Page column 52; 154-155, (2020/08/13)
Compounds of the formula (I): Q1-Q2-Q3, in which Q1, Q2 and Q3 have the meanings indicated in Claim 1, degrade target proteins, and can be employed, inter alia, for the treatment of diseases such as cancer, multiple sclerosis, cardiovascular diseases, central nervous system injury and different forms of inflammation.
Biosynthesis of defensive coccinellidae alkaloids: Incorporation of fatty acids in adaline, coccinelline, and harmonine
Haulotte, Eveline,Laurent, Pascal,Braekman, Jean-Claude
, p. 1907 - 1912 (2012/05/31)
In this study, we report on in vitro incorporation experiments of several labelled fatty acids in the ladybird alkaloids coccinelline (Coccinella 7-punctata), adaline (Adalia 2-punctata), and harmonine (Harmonia axyridis). The obtained results clearly indicate that stearic acid is the precursor of coccinelline and harmonine, whereas myristic acid is at the origin of the carbon skeleton of adaline. Possible pathways for the biosynthesis of these alkaloids are presented. In vitro incorporation experiments of labelled fatty acids in the ladybird alkaloids coccinelline (Coccinella 7-punctata), adaline (Adalia 2-punctata) and harmonine (Harmonia axyridis) indicate that stearicacid is the best precursor for the biosynthesis of coccinelline and harmonine, whereas myristic acid is more efficient for the formation of the carbon skeleton of adaline. Copyright
