134227-44-4 Usage
Uses
Used in Pharmaceutical Industry:
1-Propanol, 2-(4-phenoxyphenoxy)is used as a solvent and reagent in the pharmaceutical industry for the production of various organic compounds and pharmaceuticals. Its properties as a solvent make it suitable for dissolving and facilitating reactions in the synthesis of drugs and other medicinal products.
Used in Chemical Synthesis:
In the field of chemical synthesis, 1-Propanol, 2-(4-phenoxyphenoxy)serves as a precursor to other organic compounds. Its unique structure with two connected phenoxy groups allows it to participate in a range of chemical reactions, contributing to the creation of new compounds for various applications.
Used in Plastics and Dyes Production:
1-Propanol, 2-(4-phenoxyphenoxy)is also utilized in the production of plastics and dyes due to the aromatic nature of its phenoxy groups. These groups are commonly found in the composition of plastics and dyes, making this chemical a valuable component in their manufacturing processes.
Check Digit Verification of cas no
The CAS Registry Mumber 134227-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,2 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134227-44:
(8*1)+(7*3)+(6*4)+(5*2)+(4*2)+(3*7)+(2*4)+(1*4)=104
104 % 10 = 4
So 134227-44-4 is a valid CAS Registry Number.
134227-44-4Relevant 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.
