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2-Propen-1-one, 3-phenyl-1-selenophene-2-yl- is a complex organic compound that can be described as a derivative of 2-propen-1-one (also known as acrolein), which is a simple unsaturated aldehyde. In 2-Propen-1-one, 3-phenyl-1-selenophene-2-yl-, the acrolein molecule is modified by the attachment of a 3-phenyl-1-selenophene group. The selenophene ring is a heterocyclic compound similar to benzene but with selenium replacing one of the carbon atoms. The phenyl group attached to the selenophene ring provides additional stability and aromaticity to the molecule. 2-Propen-1-one, 3-phenyl-1-selenophene-2-yl- is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and materials with unique electronic and optical properties. Its specific applications may include the development of new pharmaceuticals, materials for electronics, or as intermediates in the synthesis of other organic compounds.

1969-62-6

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1969-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1969-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1969-62:
(6*1)+(5*9)+(4*6)+(3*9)+(2*6)+(1*2)=116
116 % 10 = 6
So 1969-62-6 is a valid CAS Registry Number.

1969-62-6Relevant academic research and scientific papers

Hetero-Diels–Alder reactions of hetaryl thiochalcones with acetylenic dienophiles

Mlostoń, Grzegorz,Grzelak, Paulina,Heimgartner, Heinz

, p. 1 - 10 (2017)

Hetaryl-substituted thiochalcones react with acetylenic mono- and diesters in the THF solution in the presence of LiClO4 at 65°C to give, after 24 h, 4H-thiopyran carboxylates and dicarboxylates, respectively, in moderate to good yields. The same reactions were performed also in the THF solution without a catalyst under microwave irradiation. In that case, the reaction time was reduced to three minutes and, in most cases, an improvement in the yield of the [4+2]-cycloadduct was observed. The reactions with methyl propiolate occurred regioselectively and the 3-carboxylates were formed exclusively.

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