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(E)-2-(3-phenylprop-2-enyl)-4,6-dimethylphenol, also known as eugenol, is a naturally occurring organic compound found in the essential oils of various plants, particularly in cloves, cinnamon, and bay leaves. It is a colorless to pale yellow oily liquid with a characteristic spicy, sweet, and slightly bitter odor. Eugenol is widely used in the food, pharmaceutical, and flavoring industries due to its antimicrobial, anti-inflammatory, and analgesic properties. It is also used as a fragrance component in perfumes and as a dental analgesic to relieve toothache. The chemical structure of eugenol consists of a phenol group with a 3-phenylprop-2-enyl side chain and two methyl groups at the 4 and 6 positions, giving it its unique properties and applications.

34591-37-2

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34591-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34591-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,9 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34591-37:
(7*3)+(6*4)+(5*5)+(4*9)+(3*1)+(2*3)+(1*7)=122
122 % 10 = 2
So 34591-37-2 is a valid CAS Registry Number.

34591-37-2Downstream Products

34591-37-2Relevant academic research and scientific papers

PROCESSES FOR THE PREPARATION OF ORTHO-ALLYLATED HYDROXY ARYL COMPOUNDS

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Paragraph 00280-00282; 00297, (2021/12/08)

The present application describes process for preparing an ortho-allylated hydroxy aryl compounds such as compounds of Formula (I) by reacting an allylic alcohol with a hydroxy aryl compound in the presence of aluminum compound selected from alumina and aluminum alkoxides and in a non-protic solvent wherein at least one carbon atom ortho to the hydroxy group in the hydroxy aryl compound is unsubstituted. The present application also includes compounds of Formula (I).

Gold-catalyzed rearrangement of substituted allyl aryl ethers

Vyvyan, James R.,Dimmitt, Heidi E.,Griffith, Jennifer K.,Steffens, Laura D.,Swanson, Rebecca A.

experimental part, p. 6666 - 6669 (2011/02/21)

Triphenylphosphinegold(I) complexes catalyze the Claisen-type rearrangement of aryl allyl ethers to the corresponding branched and linear products. The product distribution depends on the olefin geometry of the allylic ether. Stereochemical transfer experiments support an ionic mechanism.

Intramolecular excited-state interactions in phenol-styrene bicromophoric systems: A photochemical and photophysical study

Consuelo Jiménez,Miranda, Miguel A,Tormos, Rosa

, p. 115 - 120 (2007/10/03)

The intramolecular excited state interaction between phenol and styrene in a series of trans-2-cinnamylphenols bearing electron-donating substituents at the phenolic ring has been directly observed as an exciplex emission in acetonitrile. The photochemica

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