99566-46-8 Usage
Uses
Used in Pharmaceutical Industry:
(1R,2E)-1-ethyl-2-methyl-3-(3-phenoxyphenyl)prop-2-en-1-yl 4-bromobenzoate is used as a potential pharmaceutical agent for its unique structure and properties. Its complex molecular arrangement may offer novel therapeutic opportunities, although further research and testing are necessary to determine its specific uses and potential benefits.
Used in Agrochemical Industry:
In the agrochemical field, (1R,2E)-1-ethyl-2-methyl-3-(3-phenoxyphenyl)prop-2-en-1-yl 4-bromobenzoate may be utilized as a component in the development of new pesticides or herbicides. Its specific chemical structure could provide innovative solutions for crop protection and management, pending further investigation into its efficacy and safety.
Used in Materials Science:
(1R,2E)-1-ethyl-2-methyl-3-(3-phenoxyphenyl)prop-2-en-1-yl 4-bromobenzoate may also find applications in materials science, where its unique structure could be leveraged to create new materials with specialized properties. This could include uses in the development of advanced polymers, coatings, or other materials with specific characteristics tailored for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 99566-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,6 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99566-46:
(7*9)+(6*9)+(5*5)+(4*6)+(3*6)+(2*4)+(1*6)=198
198 % 10 = 8
So 99566-46-8 is a valid CAS Registry Number.
99566-46-8Relevant academic research and scientific papers
Absolute Structure and Activity Relationships of Cinnamyl Alcohol Derivatives of Pyrethroid Insecticides
Matsuo, Noritada,Yano, Toshihiko,Ohno, Nobuo
, p. 3029 - 3036 (2007/10/02)
Synthesis of three optically active pyrethroids containing cinnamyl-type alcohol moieties, and their insecticidal activity are reported.The presence of a m-phenoxy group at a benzene ring inverted the structure-activity relationships dramatically with respect to the absolute configuration of alcohol moieties.
