88355-77-5 Usage
Uses
Used in Chemical Research:
(1E)-N-[4-(4-phenoxyphenoxy)butoxy]propan-1-imine is used as a research compound for studying its chemical properties and potential applications in various fields.
Used in Pharmaceutical Development:
(1E)-N-[4-(4-phenoxyphenoxy)butoxy]propan-1-imine is used as a building block in the synthesis of new pharmaceutical compounds, potentially contributing to the development of novel drugs.
Used in Drug Synthesis:
(1E)-N-[4-(4-phenoxyphenoxy)butoxy]propan-1-imine is used as a key intermediate in the synthesis of various drug molecules, facilitating the creation of new therapeutic agents.
Used in Industrial Processes:
(1E)-N-[4-(4-phenoxyphenoxy)butoxy]propan-1-imine may be utilized in various industrial processes, such as the production of specialty chemicals or materials, depending on its specific properties and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 88355-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,5 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88355-77:
(7*8)+(6*8)+(5*3)+(4*5)+(3*5)+(2*7)+(1*7)=175
175 % 10 = 5
So 88355-77-5 is a valid CAS Registry Number.
88355-77-5Relevant academic research and scientific papers
Oxime Ethers: New Potent Insect Growth Regulators
Ohsumi, Tadashi,Hatakoshi, Makoto,Kisida, Hirosi,Matsuo, Noritada,Nakayama, Isamu,Itaya, Nobushige
, p. 3197 - 3202 (2007/10/02)
Oxime ethers containing a 4-phenoxyphenoxy group in the molecules were synthesized and their insect growth regulating (IGR) activities were studied.Of these new IGR's, propionaldehyde oxime O-2-(4-phenoxyphenoxy)ethyl ether and propionaldehyde oxime O-2-(phenoxyphenoxy)propyl ether were found to be most effective, having much higher activities than methoprene against larvae of Culex pipiens pallens and Musca domestica by the immersion method and medium method, respectively.In addition, the effects of steric isomerism of these compounds were examined; their IGR activities were found to have a close relationship to the juvenile hormone activity by the Galleria wax test.
