663603-70-1 Usage
Description
(2Z)-3-(METHYLAMINO)-1-(2-THIENYL)PROP-2-EN-1-ONE, also known as 2-methylamino-1-(2-thienyl)but-2-en-1-one, is a yellow to brown liquid with a strong odor. It belongs to the class of organic compounds known as thienylketones, which are compounds containing a ketone group substituted by a thienyl group. This chemical is characterized by its semiconducting properties and is used in various industrial applications.
Uses
Used in Pharmaceutical Industry:
(2Z)-3-(METHYLAMINO)-1-(2-THIENYL)PROP-2-EN-1-ONE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs.
Used in Pesticide Industry:
(2Z)-3-(METHYLAMINO)-1-(2-THIENYL)PROP-2-EN-1-ONE is used as a component in the production of pesticides, leveraging its chemical properties to enhance the effectiveness of these agricultural chemicals.
Used in Organic Synthesis:
(2Z)-3-(METHYLAMINO)-1-(2-THIENYL)PROP-2-EN-1-ONE is used as a reagent in organic synthesis processes, facilitating the creation of a variety of organic compounds for different applications.
Used in Organic Photovoltaics:
(2Z)-3-(METHYLAMINO)-1-(2-THIENYL)PROP-2-EN-1-ONE is used as a semiconducting material in the field of organic photovoltaics, where its properties contribute to the efficiency and performance of solar cells.
It is crucial to handle (2Z)-3-(METHYLAMINO)-1-(2-THIENYL)PROP-2-EN-1-ONE with care due to its potential hazards if not properly managed or utilized.
Check Digit Verification of cas no
The CAS Registry Mumber 663603-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,3,6,0 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 663603-70:
(8*6)+(7*6)+(6*3)+(5*6)+(4*0)+(3*3)+(2*7)+(1*0)=161
161 % 10 = 1
So 663603-70-1 is a valid CAS Registry Number.
663603-70-1Relevant articles and documents
An efficient method for the synthesis of 2-pyridones: Via C-H bond functionalization
Zhou, Shuguang,Liu, Duan-Yang,Wang, Suo,Tian, Jie-Sheng,Loh, Teck-Peng
supporting information, p. 15020 - 15023 (2020/12/23)
A simple and practical method to access N-substituted 2-pyridones via a formal [3+3] annulation of enaminones with acrylates based on RhIII-catalyzed C-H functionalization was developed. Control and deuterated experiments led to a plausible mechanism involving C-H bond cross-coupling and aminolysis cyclization. This strategy provides a short synthesis of structural motifs of N-substituted 2-pyridones.
(E)-N-MONOALKYL-3-OXO-3-(2-THIENYL)PROPENAMINE AND PROCESS FOR PRODUCING THE SAME AND (E,Z)-N-MONOALKYL-3-OXO-3-(2-THIENYL)PROPENAMINE AND PROCESS FOR PRODUCING THE SAME
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Page/Page column 12-13, (2008/06/13)
It is intended to provide a process for producing (E)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine represented by the general formula (I): (wherein R represents an alkyl group having 1 to 4 carbon atoms), characterized by maintaining a solution in which (Z)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine is dissolved in a solvent at 25°C or lower thereby to deposit crystals and fractionating a crystal with a particle size of 100 μm or less from the deposited crystals; and a process for producing (E,Z)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine, characterized by adding a water-insoluble organic solvent to a reaction solution obtained by reacting an alkali metal salt of β-oxo-β-(2-thienyl) propanal with a monoalkylamine compound, adding a seed crystal containing (E)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine to an organic layer obtained by separation and maintaining the temperature at 25°C or lower.
