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192193-84-3

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192193-84-3 Usage

Description

2,5-Cyclohexadien-1-one,4-hydroxy-4-(1-methylethyl)-(9CI), also known as 4-(1-Methylethyl)-4-hydroxy-2-cyclohexen-1-one, is a chemical compound with the molecular formula C10H12O2. It is a yellow liquid characterized by a fruity, honey-like odor and is commonly found in fruits such as apple, banana, and cherry. 2,5-Cyclohexadien-1-one,4-hydroxy-4-(1-methylethyl)-(9CI) is widely used as a flavoring agent and fragrance ingredient in various industries.

Uses

Used in Flavor and Fragrance Industry:
2,5-Cyclohexadien-1-one,4-hydroxy-4-(1-methylethyl)-(9CI) is used as a flavoring agent for its fruity, honey-like aroma, adding a natural scent to food products and enhancing their taste.
Used in Perfume Production:
2,5-Cyclohexadien-1-one,4-hydroxy-4-(1-methylethyl)-(9CI) is used as a fragrance ingredient in the production of perfumes, contributing to the creation of complex and pleasant scents.
Used in Cosmetics Industry:
2,5-Cyclohexadien-1-one,4-hydroxy-4-(1-methylethyl)-(9CI) is used in cosmetics for its pleasant odor, enhancing the sensory experience of the products and providing a natural scent.
Used in Food Products:
2,5-Cyclohexadien-1-one,4-hydroxy-4-(1-methylethyl)-(9CI) is used in the food industry as a flavoring agent, imparting a fruity and honey-like taste to various food items, thereby improving their overall flavor profile.
Used in Medicinal Applications:
2,5-Cyclohexadien-1-one,4-hydroxy-4-(1-methylethyl)-(9CI) has been studied for its potential medicinal uses, such as its antioxidant and anti-inflammatory properties, indicating its potential as a therapeutic agent in the development of new drugs.
It is important to handle 2,5-Cyclohexadien-1-one,4-hydroxy-4-(1-methylethyl)-(9CI) with care, as it can cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken during its use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 192193-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,1,9 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 192193-84:
(8*1)+(7*9)+(6*2)+(5*1)+(4*9)+(3*3)+(2*8)+(1*4)=153
153 % 10 = 3
So 192193-84-3 is a valid CAS Registry Number.

192193-84-3Downstream Products

192193-84-3Relevant articles and documents

Chemistry of 4-alkylaryloxenium ion "precursors": Sound and fury signifying something?

Novak, Michael,Brinster, Aaron M.,Dickhoff, Jill N.,Jones, Matthew P.,Leopold, Samuel H.,Vollman, Andrew T.,Wang, Yue-Ting,Glover, Stephen A.

, p. 9954 - 9962 (2008/09/18)

(Chemical Equation Presented) Quinol esters 2b, 2c, and 3b and sulfonamide 4c were investigated as possible precursors to 4-alkylaryloxenium ions, reactive intermediates that have not been previously detected. These compounds exhibit a variety of interesting reactions, but with one possible exception, they do not generate oxenium ions. The 4-isopropyl ester 2b predominantly undergoes ordinary acid- and base-catalyzed ester hydrolysis. The 4-tert-butyl ester 2c decomposes under both acidic and neutral conditions to generate tert-butanol and 1-acetyl-1,4-hydroquinone, 8, apparently by an SN1 mechanism. This is also a minor decomposition pathway for 2b, but the mechanism in that case is not likely to be SN1. Decomposition of 2c in the presence of N 3- leads to formation of the explosive 2,3,5,6-tetraazido-1,4-benzoquinone, 14, produced by N3 -induced hydrolysis of 8, followed by a series of oxidations and nucleophilic additions by N3 . No products suggestive of N3--trapping of an oxenium ion were detected. The 4-isopropyl dichloroacetic acid ester 3b reacts with N3- to generate the two adducts 2-azido-4-isopropylphenol, 5b, and 3-azido-4-isopropylphenol, 11b. Although 5b is the expected product of N3- trapping of the oxenium ion, kinetic analysis shows that it is produced by a kinetically bimolecular reaction of N3- with 3b. No oxenium ion is involved. The sulfonamide 4c predominantly undergoes a rearrangement reaction under acidic and neutral conditions, but a minor component of the reaction yields 4-tert-butylcresol, 17, and 2-azido-4-tert-butylphenol, 5c, in the presence of N3-. These products may indicate that 4c generates the oxenium ion 1c, but they are generated in very low yields (ca. 10%) so it is not possible to definitively conclude that 1c has been produced. If 1c has been generated, the N3--trapping data indicate that it is a very short-lived and reactive species in H2O. Comparisons with similarly reactive nitrenium ions indicate that the lifetime of 1c is ca. 20-200 ps if it is generated, so it must react by a preassociation process. Density functional theory calculations at the B3LYP/6-31G*//HF/6-31G* level coupled with kinetic correlations also indicate that the aqueous solution lifetimes of 1a-c are in the picosecond range.

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