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2,4-diallyl-4-methylcyclohexa-2,5-dien-1-one is a complex organic compound with the molecular formula C12H16O. It is a colorless to pale yellow liquid with a strong, pungent odor. This chemical is a member of the cyclohexenone family and is characterized by its unique structure, which includes a cyclohexane ring with a carbonyl group at position 1, a methyl group at position 4, and two allyl groups at positions 2 and 4. It is synthesized through various chemical reactions and is used in the production of fragrances and flavorings, particularly in the creation of jasmine and other floral scents. Due to its reactive nature, it is important to handle 2,4-diallyl-4-methylcyclohexa-2,5-dien-1-one with care, following proper safety protocols.

2059-44-1

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2059-44-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2059-44-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2059-44:
(6*2)+(5*0)+(4*5)+(3*9)+(2*4)+(1*4)=71
71 % 10 = 1
So 2059-44-1 is a valid CAS Registry Number.

2059-44-1Downstream Products

2059-44-1Relevant academic research and scientific papers

Pd-catalyzed C4-Dearomative Allylation of Benzyl Ammoniums with Allyltributylstannane

Kayashima, Yuki,Komatsuda, Masaaki,Muto, Kei,Yamaguchi, Junichiro

, p. 836 - 839 (2020)

A dearomative C4-allylation of benzyl ammoniums with allyltributylstannane by a palladium catalysis is described. A triarylphosphine-ligated palladium catalyst, which is capable of cleaving benzylic CN bonds, realized facile dearomative reactions with C4 selectivity. Combined with precedented C2- A nd C3-selective functionalizations of benzyl amine derivatives, the present reaction can provide a new synthetic option for the synthesis of multi-substituted alicyclic compounds as well as aromatic compounds.

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