25328-90-9 Usage
Description
(1E)-1-phenylcyclooctene, a member of the cycloalkene family, is a chemical compound with the molecular formula C16H20. It features a phenyl group attached to a cyclooctene ring, and the "1E" notation in its name signifies the position of the double bond within the molecule. (1E)-1-phenylcyclooctene is valued for its versatile nature and unique structural properties, making it a promising candidate for researchers and chemists in the development of new compounds and materials.
Uses
Used in Organic Synthesis:
(1E)-1-phenylcyclooctene is utilized as a building block in organic synthesis, providing a foundation for the creation of more complex organic molecules. Its unique structure allows for various chemical reactions to be performed, facilitating the synthesis of a wide range of compounds.
Used in Pharmaceutical Production:
(1E)-1-phenylcyclooctene serves as a starting material for the production of pharmaceuticals. Its structural properties make it suitable for the development of new drugs, potentially leading to advancements in medicine and healthcare.
Used in Agrochemical Production:
(1E)-1-phenylcyclooctene also finds application in the agrochemical industry, where it is used as a starting material for the synthesis of various agrochemicals. Its role in this industry is crucial for the development of new products that can improve agricultural practices and crop protection.
Used in Specialty Chemicals:
(1E)-1-phenylcyclooctene is employed in the production of specialty chemicals, which are often used in niche applications across different industries. Its unique properties contribute to the development of innovative and specialized chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 25328-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,2 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25328-90:
(7*2)+(6*5)+(5*3)+(4*2)+(3*8)+(2*9)+(1*0)=109
109 % 10 = 9
So 25328-90-9 is a valid CAS Registry Number.
25328-90-9Relevant articles and documents
Iodobenzene-catalyzed oxidative cleavage of olefins to carbonyl compounds
Du, Lele,Wang, Zechao,Wu, Junliang
, (2020/07/20)
A metal-free approach for the oxidative cleavage of carbon–carbon double bonds of olefins to carbonyl compounds was established by using oxidant m-CPBA and non-metallic organocatalyst PhI in toluene/H2O. A broad scope of aromatic olefins was used. All the reactions proceeded smoothly at 35 °C in short reaction time to furnish the respective mono- and double carbonyl compounds selectively in moderate to good yields.
Triphosgene and DMAP as Mild Reagents for Chemoselective Dehydration of Tertiary Alcohols
Ganiu, Moshood O.,Cleveland, Alexander H.,Paul, Jarrod L.,Kartika, Rendy
supporting information, p. 5611 - 5615 (2019/08/01)
The utility of triphosgene and DMAP as mild reagents for chemoselective dehydration of tertiary alcohols is reported. Performed in dichloromethane at room temperature, this reaction is readily tolerated by a broad scope of substrates, yielding alkenes preferentially with the (E)-geometry. While formation of the Hofmann products is generally favored, a dramatic change in alkene selectivity toward the Zaitzev products is observed when the reaction is carried out in dichloroethane at reflux.
Efficient functionalization of olefins by arylsilanes catalyzed by palladium anionic complexes
Silarska,Majchrzak,Marciniec,Trzeciak
, p. 458 - 464 (2016/12/16)
The coupling of organosilanes and different olefins was performed efficiently in the presence of anionic complexes, [CA]2[PdX4] and [CA]2[Pd2X6], where CA?=?imidazolium or pyridinium cation. The reaction proceeds according to a Pd(II)-mediated pathway, and Cu(OAc)2 acts as the re-oxidant of Pd(0) formed during the catalytic process. High product yields were obtained for differently substituted olefins at 80?°C in 4?h. Styrylsilanes reacted in the same conditions giving unsymmetrical 1,3-dienes.
