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(1E)-N-[3-(4-phenoxyphenoxy)propoxy]propan-1-imine is a complex organic chemical compound characterized by its molecular formula C21H23NO2. It features an imine functional group, which is a carbon-nitrogen double bond, and a distinctive long hydrocarbon chain with a phenoxyphenoxy group attached. (1E)-N-[3-(4-phenoxyphenoxy)propoxy]propan-1-imine is known for its potential applications across various fields, including organic synthesis, pharmaceuticals, agrochemicals, and materials science, where it serves as a reactant or intermediate. Given its intricate structure and reactivity, careful handling and storage are essential to avoid degradation or unintended chemical reactions.

88355-74-2

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88355-74-2 Usage

Uses

Used in Organic Synthesis:
(1E)-N-[3-(4-phenoxyphenoxy)propoxy]propan-1-imine is utilized as a reactant or intermediate in organic synthesis, playing a crucial role in the formation of more complex organic molecules. Its unique structure allows it to participate in various chemical reactions, contributing to the synthesis of a wide range of compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (1E)-N-[3-(4-phenoxyphenoxy)propoxy]propan-1-imine may be employed as a building block for the development of new drugs. Its specific chemical properties could be harnessed to create molecules with therapeutic potential, targeting a variety of medical conditions.
Used in Agrochemicals:
(1E)-N-[3-(4-phenoxyphenoxy)propoxy]propan-1-imine could also find applications in the agrochemical industry, where it might be used to develop new pesticides, herbicides, or other agricultural chemicals. Its reactivity and structural features could be key in creating effective compounds for crop protection and enhancement.
Used in Materials Science:
Within the realm of materials science, this imine compound might be explored for its potential to contribute to the development of new materials with unique properties. Its ability to form part of complex molecular structures could lead to advances in areas such as polymer science, nanotechnology, or the creation of novel materials with specific characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 88355-74-2 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 88355-74:
(7*8)+(6*8)+(5*3)+(4*5)+(3*5)+(2*7)+(1*4)=172
172 % 10 = 2
So 88355-74-2 is a valid CAS Registry Number.

88355-74-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-N-[3-(4-phenoxyphenoxy)propoxy]propan-1-imine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88355-74-2 SDS

88355-74-2Downstream Products

88355-74-2Relevant 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.

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