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1,4-Pentadien-3-one, 1-phenyl-5-(trimethylsilyl)-, (E,E)- is a complex organic compound with the molecular formula C14H20OSi. It is characterized by a pentadienone core, which consists of a five-carbon chain with alternating double bonds, and a carbonyl group at the third position. The molecule features a phenyl group attached to the first carbon and a trimethylsilyl group at the fifth carbon. The (E,E)- configuration indicates that both double bonds have the same geometric arrangement, with the phenyl and trimethylsilyl groups on the same side of the molecule. 1,4-Pentadien-3-one, 1-phenyl-5-(trimethylsilyl)-, (E,E)- is primarily used in organic synthesis and as a chemical intermediate, particularly in the preparation of various pharmaceuticals and specialty chemicals. Its unique structure and reactivity make it a valuable building block in the synthesis of more complex molecules.

59376-62-4

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59376-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59376-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,7 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59376-62:
(7*5)+(6*9)+(5*3)+(4*7)+(3*6)+(2*6)+(1*2)=164
164 % 10 = 4
So 59376-62-4 is a valid CAS Registry Number.

59376-62-4Downstream Products

59376-62-4Relevant academic research and scientific papers

Silicon-Directed Nazarov Reactions II. Preparation and Cyclization of β-Silyl-substituted Divinyl Ketones

Jones, Todd K.,Denmark, Scott E.

, p. 2377 - 2396 (2007/10/02)

Two general methods for the preparation of β-silyl-substituted divinyl ketones have been developed starting from either α,β-unsaturated aldehydes or simple ketones.Anhydrous FeCl3 induces the cyclization to cyclopentenones under mild conditions and in good yields with predictable and complete control over the position of the double bond in the five-membered ring.The observed effects of substituents on rate can be explained by a rate-determining cationic electrocyclization.Silyl substitution has been shown to retard the reaction.

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