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(2E,4E)-11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid is a chemical compound that belongs to the class of dodeca-2,4-dienoic acids. It is characterized by the presence of methoxy, methyl, and double bond functional groups in its structure. (2E,4E)-11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid is known for its potential biological and pharmacological activities, including anti-inflammatory, antimicrobial, and antifungal properties. It is also used in the research and development of new drugs and therapeutic agents. Overall, (2E,4E)-11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid has significant potential for various applications in the fields of medicine, pharmaceuticals, and biotechnology.

207597-76-0

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207597-76-0 Usage

Uses

Used in Pharmaceutical Industry:
(2E,4E)-11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid is used as a pharmaceutical agent for its anti-inflammatory, antimicrobial, and antifungal properties. It can be utilized in the development of new drugs and therapeutic agents to treat various diseases and infections.
Used in Biotechnology Industry:
(2E,4E)-11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid is used as a research compound in biotechnology for exploring its potential biological and pharmacological activities. It can contribute to the discovery of new treatments and therapies for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 207597-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,5,9 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 207597-76:
(8*2)+(7*0)+(6*7)+(5*5)+(4*9)+(3*7)+(2*7)+(1*6)=160
160 % 10 = 0
So 207597-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H28O3/c1-13(10-7-11-16(3,4)19-5)8-6-9-14(2)12-15(17)18/h6,9,12-13H,7-8,10-11H2,1-5H3,(H,17,18)/b9-6+,14-12-/t13-/m1/s1

207597-76-0Downstream Products

207597-76-0Relevant academic research and scientific papers

FORMULATIONS FOR THE DELIVERY OF ACTIVE AGENTS TO INSECTS, PLANTS, AND PLANT PATHOGENS

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Paragraph 0300; 0301, (2017/12/07)

The present disclosure is directed to formulations comprising (1) at least one formulation transport agent, (2) at least one complexing agent, and (3) at least one active agent that modulates one or more traits of a target insect, plant, or plant pathogen. The present disclosure is also directed to methods of delivering such formulations to the target organism, as well as to formulation transport agents used to prepare such formulations.

Photoproducts and metabolites of a common insect growth regulator produce developmental deformities in Xenopus

La Clair, James J.,Bantle, John A.,Dumont, James

, p. 1453 - 1461 (2007/10/03)

In the past decade, numerous sights across North America have been found which contain abnormal levels of deformed amphibians. This deformation was not limited to species, geography, or climate and spanned a wide range of phenotypes. This report begins to explain these findings by examining the effects of pesticide degradation in early amphibian development through directly exposing Xenopus laevis embryos to trace levels of synthetically prepared degradates. This method specifically determines the risk posed by each individual chemical resulting from the natural fate of the host pesticide. Through this approach, we find that while the common insect growth regulator, S-methoprene, poses minimal developmental determent, products of its reaction with sunlight, water, and microorganisms dramatically interfere with normal amphibian development. The addition of 1 μL/L of several of S- methoprene's degradates to the environment of developing embryos resulted in juveniles with deformation similar to that found naturally. Current developmental assessments examine only the risk posed by host pesticides. This study now suggest that the simple examination of the these materials is not sufficient, but now forward the need for critically examining the temporal relation between both development and chemical degradation. In the past decade, numerous sights across North America have been found which contain abnormal levels of deformed amphibians. This deformation was not limited to species, geography, or climate and spanned a wide range of phenotypes. This report begins to explain these findings by examining the effects of pesticide degradation in early amphibian development through directly exposing Xenopus laevis embryos to trace levels of synthetically prepared degradates. This method specifically determines the risk posed by each individual chemical resulting from the natural fate of the host pesticide. Through this approach, we find that while the common insect growth regulator, S-methoprene, poses minimal developmental determent, products of its reaction with sunlight, water, and microorganisms dramatically interfere with normal amphibian development. The addition of 1 μL/L of several of S-methoprene's degradates to the environment of developing embryos resulted in juveniles with deformation similar to that found naturally. Current developmental assessments examine only the risk posed by host pesticides. This study now suggest that the simple examination of the these materials is not sufficient, but now forward the need for critically examining the temporal relation between both development and chemical degradation.

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