25226-98-6 Usage
Description
(E)-(3,3-diethoxy-1-propenyl)benzene, also known as chavicol, is a phenylpropanoid compound that is a colorless to pale yellow liquid with a strong, sweet, and spicy odor.
Uses
Used in Perfume Industry:
(E)-(3,3-diethoxy-1-propenyl)benzene is used as a fragrance ingredient for its strong, sweet, and spicy scent.
Used in Food Industry:
(E)-(3,3-diethoxy-1-propenyl)benzene is used as a flavoring agent to enhance the taste and aroma of various food products.
Used in Traditional Medicine:
(E)-(3,3-diethoxy-1-propenyl)benzene is used for its antimicrobial and antifungal properties to treat various ailments.
Used in Cosmetics Manufacturing:
(E)-(3,3-diethoxy-1-propenyl)benzene is used in the production of cosmetics for its pleasant odor and potential antimicrobial properties.
Used in Insecticides:
(E)-(3,3-diethoxy-1-propenyl)benzene is used in the formulation of insecticides to control and repel insects.
Note: Handle (E)-(3,3-diethoxy-1-propenyl)benzene with caution as it may cause skin and eye irritation, and it should be used in well-ventilated areas.
Check Digit Verification of cas no
The CAS Registry Mumber 25226-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,2 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25226-98:
(7*2)+(6*5)+(5*2)+(4*2)+(3*6)+(2*9)+(1*8)=106
106 % 10 = 6
So 25226-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O2/c1-3-14-13(15-4-2)11-10-12-8-6-5-7-9-12/h5-11,13H,3-4H2,1-2H3/b11-10+
25226-98-6Relevant articles and documents
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Alexakis,A. et al.
, p. 2313 - 2316 (1976)
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Tropylium salts as efficient organic Lewis acid catalysts for acetalization and transacetalization reactions in batch and flow
Lyons,Crocker,Enders,Nguyen
supporting information, p. 3993 - 3996 (2017/09/08)
Acetalization reactions play significant roles in the synthetically important masking chemistry of carbonyl compounds. Herein we demonstrate for the first time that tropylium salts can act as organic Lewis acid catalysts to facilitate acetalization and transacetalization reactions of a wide range of aldehyde substrates. This metal-free method works efficiently in both batch and flow conditions, prompting further future applications of tropylium organocatalysts in green synthesis.
Generation and stereoselective transformations of 3-phenylcyclopropene
Sheshenev, Andrey E.,Baird, Mark S.,Croft, Anna K.,Bolesov, Ivan G.
experimental part, p. 10036 - 10046 (2010/02/27)
A convenient and inexpensive approach to the generation of 3-phenylcyclopropenes is described. Reaction of these compounds with a range of dienophiles and dipolarophiles led to the stereoselective formation of [4+2]- and [3+2]-cycloadducts, which were exclusively exo-3-phenyl-cis-1,2-disubstituted cyclopropanes. Efficient trapping of 1-lithio-3-phenylcyclopropene with different electrophiles is also discussed. Ab initio calculations suggest that the lowest energy conformation of 3-phenylcyclopropene has the plane of the benzene ring perpendicular to the cyclopropene π-bond but with a low rotation barrier.
