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(Z)-3-(4-Chloro-phenylselanyl)-1-phenyl-prop-2-en-1-ol is a complex organic compound characterized by its unique molecular structure. It features a phenylselanyl group, which is a phenyl ring bonded to a selenium atom, attached to the 3-position of a prop-2-en-1-ol backbone. The phenyl ring at the 1-position and the chlorine atom at the 4-position of the phenylselanyl group contribute to its distinct chemical properties. (Z)-3-(4-Chloro-phenylselanyl)-1-phenyl-prop-2-en-1-ol is of interest in the field of organic chemistry, particularly in the study of selenium-containing compounds, which can exhibit unique reactivity and stability. Its potential applications may span across various chemical and pharmaceutical industries, where such structurally diverse molecules are often explored for their specific properties and potential uses.

74824-80-9

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74824-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74824-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,2 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74824-80:
(7*7)+(6*4)+(5*8)+(4*2)+(3*4)+(2*8)+(1*0)=149
149 % 10 = 9
So 74824-80-9 is a valid CAS Registry Number.

74824-80-9Downstream Products

74824-80-9Relevant academic research and scientific papers

Reactions of 3-Hydroxyvinyl Selenones with Alkoxides. Oxetane Formation and Fragmentation Reactions

Shimizu, Makoto,Ando, Ryoichi,Kuwajima, Isao

, p. 1230 - 1238 (2007/10/02)

3-Hydroxyvinyl phenyl selenones are prepared and their behavior as conjugate addition acceptors has been investigated.As a result, a selenonyl group has been found to activate the C=C bond for conjugate addition of nucleophiles and further to behave as an

3-(Phenylseleno)-2-propenal as a Versatile Unit for Oxetane Ring Formation

Shimizu, Makoto,Kuwajima, Isao

, p. 4063 - 4065 (2007/10/02)

Treatment of 1-alkyl-3-(phenylseleno)-2-propen-1-ol with 2 equiv of MCPBA followed by sodium hydroxide in aqueous methanol gave 2-alkyl-3-methoxyoxetane in good yield.

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