7389-19-7 Usage
Description
(E)-(4-aminophenyl)(4'-chlorophenyl)ethene, also known as 4'-chloro-α-methylstyrene, is a chemical compound with the molecular formula C14H12ClN. It is a styrene derivative with a chlorine atom at the 4' position and an amino group at the 4 position on the phenyl ring. This versatile compound has been studied for its potential use in the development of pharmaceuticals and agrochemicals, as well as its role in organic synthesis and material science.
Uses
Used in Pharmaceutical Development:
(E)-(4-aminophenyl)(4'-chlorophenyl)ethene is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, (E)-(4-aminophenyl)(4'-chlorophenyl)ethene is utilized as a building block for the creation of novel agrochemicals. Its properties make it suitable for the design of pesticides and other agricultural chemicals that can improve crop yields and protect plants from pests.
Used in Organic Synthesis:
(E)-(4-aminophenyl)(4'-chlorophenyl)ethene serves as a valuable reactant in organic synthesis, enabling the production of a wide range of organic compounds. Its reactivity and functional groups make it a useful component in the synthesis of various organic molecules.
Used in Material Science:
In the field of material science, (E)-(4-aminophenyl)(4'-chlorophenyl)ethene is employed in the development of new materials with unique properties. Its structural features contribute to the creation of materials with potential applications in various industries, such as electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 7389-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7389-19:
(6*7)+(5*3)+(4*8)+(3*9)+(2*1)+(1*9)=127
127 % 10 = 7
So 7389-19-7 is a valid CAS Registry Number.
7389-19-7Relevant articles and documents
Xanthate-mediated synthesis of (E)-alkenes by semi-hydrogenation of alkynes using water as the hydrogen donor
Luo, Xianglin,Chen, Xiuwen,Chen, Lu,Zhang, Kun,Li, Yibiao
supporting information, p. 2170 - 2173 (2019/02/24)
Semi-hydrogenation of alkynes is one of the most widely used methods for obtaining alkenes in laboratory preparation and in industry. Transition metal catalysts have been extensively studied for this transformation, but the tolerance of functional groups, such as pyridine,-OH,-NH2,-Bpin, and halides, and the toxicity of the trace amount of transition metal catalysts are still highly challenging. In this study, we report a general and robust strategy to achieve the semi-hydrogenation of alkynes using inexpensive and commercially available xanthate as the mediator. Mechanism studies support a non-radical process and H2O acts as the hydrogen donor.
Spectroscopic Correlations between Supermolecules and Molecules. Anatomy of the Ion-Modulated Electronic Properties of the Nitrogen Donor in Monoazacrown-Derived Intrinsic Fluoroionophores
Yang, Jye-Shane,Hwang, Chung-Yu,Hsieh, Chia-Chun,Chiou, Shih-Yi
, p. 719 - 726 (2007/10/03)
The synthesis, absorption and emission spectra, fluorescence quantum yields, and fluorescence lifetimes of three compound series of trans-4,4′-disubstituted aminostilbenes (1-3) are reported. The chromo-/fluoroionophoric behavior of the monoaza-15-crown-5
