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3-(4-methoxyphenyl)hex-5-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78303-43-2

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78303-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78303-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,0 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78303-43:
(7*7)+(6*8)+(5*3)+(4*0)+(3*3)+(2*4)+(1*3)=132
132 % 10 = 2
So 78303-43-2 is a valid CAS Registry Number.

78303-43-2Downstream Products

78303-43-2Relevant academic research and scientific papers

The salt-free nickel-catalysed α-allylation reaction of ketones with allyl alcohol and diallylether

Mouhsine, Bouchaib,Karim, Abdallah,Dumont, Clément,Sauthier, Mathieu

supporting information, p. 950 - 955 (2020/02/25)

The nickel-catalysed α-allylation of ketones with allyl alcohol and diallylether has been performed under neutral conditions. As no base is involved, the products are synthesized without salts as side products. The dppf/Ni(cod)2 catalytic system in MeOH at 80 °C has been shown as the most effective reaction system to afford tetrasubstituted derivatives from various cyclic and acyclic ketones with one or two mobile protons. This process combined with a metathesis step yields spirocyclic compounds according to a salt free synthetic sequence.

Platinum(IV)-Catalyzed Synthesis of Unsymmetrical Polysubstituted Benzenes via Intramolecular Cycloaromatization Reaction

Zheng, Shuyan,Zhang, Jinghua,Shen, Zhengwu

supporting information, p. 2803 - 2808 (2015/09/28)

A one-pot synthesis of polysubstituted benzene derivatives was achieved via a platinum(IV)-catalyzed intramolecular cycloaromatization reaction. The reaction proceeds via a tandem skeletal rearrangment, dehydration and double bond isomerization, which proved to be very useful for the syntheses of a range of interesting polyalkyl-substituted benzenes.

Nucleophilic α-arylation and α-alkylation of ketones by polarity inversion of N-alkoxyenamines: Entry to the umpolung reaction at the α-carbon position of carbonyl compounds

Miyoshi, Tetsuya,Miyakawa, Takayuki,Ueda, Masafumi,Miyata, Okiko

supporting information; experimental part, p. 928 - 931 (2011/04/14)

A new aspect of enamine chemistry: The formation of N-alkoxyenamines from ketones has led to an efficient umpolung reaction. The alkylation of N-alkoxyenamines with trialkylaluminum compounds proceeded smoothly and gave α-alkylated ketones (see scheme). This reaction offers a simple transformation of ketones into α-substituted ketones without the need to isolate enamines and intermediary imines.

REACTION OF ALLYLSILANE WITH α-NITRO OLEFIN AND ITS DEVELOPMENT TO SYNTHESIS OF CYCLOPENTENONE

Ochiai, Masahito,,Arimoto, Masao,Fujita, Eiichi

, p. 1115 - 1118 (2007/10/02)

Michael addition of allylsilane to α-nitro olefin in the presence of AlCl3 proceeded smoothly at low temperature to give unsaturated nitronic acid, which was converted into the γδ-enone using aqueous Ti (III).Transformation of the enone into the 1,4-diketone followed by the intramolecular aldol condensation with the latter provided a convenient new synthesis of cyclopentanone.

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