75069-38-4

Usage

Uses

Used in Fragrance Industry:
Ethanone, 1-[5-(1,1-dimethylethyl)-2-methoxyphenyl]is used as a fragrance compound for its strong, sweet, balsamic scent. It is incorporated into perfumes and cosmetics to provide a pleasant aroma that enhances the sensory experience of these products.
Used in Personal Care Products:
In the personal care industry, Ethanone, 1-[5-(1,1-dimethylethyl)-2-methoxyphenyl]is used as a scenting agent in soaps, shampoos, and other products. Its pleasant odor makes it a desirable ingredient for creating appealing and enjoyable personal care formulations.
Used in Skincare Products:
Ethanone, 1-[5-(1,1-dimethylethyl)-2-methoxyphenyl]has been studied for its potential antioxidant and anti-inflammatory properties. As a result, it is considered a potentially valuable ingredient in skincare products, where it may contribute to the maintenance of skin health and the reduction of inflammation.
Used in Antioxidant Formulations:
Due to its antioxidant properties, Ethanone, 1-[5-(1,1-dimethylethyl)-2-methoxyphenyl]can be used in formulations designed to protect the skin from oxidative stress and environmental damage. Its inclusion in skincare products may help to preserve the integrity of the skin and support its natural defenses against aging and other skin conditions.
Used in Anti-Inflammatory Formulations:
The anti-inflammatory properties of Ethanone, 1-[5-(1,1-dimethylethyl)-2-methoxyphenyl]make it suitable for use in formulations aimed at reducing inflammation and soothing irritated skin. It may be particularly beneficial in products designed for sensitive or reactive skin types, providing relief and support for skin health.

Upstream product

• 5396-38-3 1-(tert-butyl)-4-methoxybenzene 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 

Downstream Products

• 182007-02-9 1,1-Bis-(5-tert-butyl-2-methoxy-phenyl)-ethanol 
• 1397286-79-1 (E)-2,3-bis(5-tert-butyl-2-methoxylphenyl)-2-butene 
• 1397286-80-4 (Z)-2,3-bis(5-tert-butyl-2-methoxylphenyl)-2-butene 
• 182007-08-5 1,1-bis(5-tert-butyl-2-methoxyphenyl)ethane 
• 182007-05-2 1,1-bis(5-tert-butyl-2-methoxyphenyl)ethene 
• 855165-52-5 2-(5-tert-butyl-2-methoxy-phenyl)-quinoline-4-carboxylic acid 

Relevant academic research and scientific papers

Synthesis and structure of 2,3-bis(5-tert-butyl-2-methoxyphenyl)buta-1,3- diene by bromine elimination of-1,4-dibromo-2,3-bis(5-tert-butyl-2- methoxyphenyl)-2-butene

2,3-Bis(5-tert-butyl-2-methoxyphenyl)buta-1,3-diene was prepared by bromination of (Z)-and (E)-2,3-bis(5-tert-butyl-2-methoxyphenyl)-2-butene followed by treatment with zinc powder in a mixture of CH2Cl2 and acetic acid, which was converted to the corresponding o-terphenyl skeleton by the condensation with dimethyl acetylenedicarboxylate followed by oxidation with 2,3-dichloro-5,6-dicyanobenzoquinone.

2-Acyl-6-aminomethylphenol derivatives

A 2-acyl-6-aminomethylphenol derivative having the formula (I): STR1 wherein R1 represents a straight chain or branched chain alkyl group of 1 to 6 carbon atoms unsubstituted or substituted with 1 to 3 halogen atoms; a hydrogen atom or a group having the formula (II): wherein n represents 0 or an integer of 1 to 6; R7 represents a cycloalkyl group of 3 to 8 carbon atoms unsubstituted or substituted with at least one lower alkyl group; a phenyl group unsubstituted or substituted with at least one lower alkyl group, a halogen atom, a lower alkoxy group or a lower alkylthio group; a lower alkoxy group; a lower alkylthio group; a lower alkylsulfinyl group; a lower alkylsulfonyl group; an N-lower alkylamino group; an N,N-di-lower alkylamino group; or a pyridyl, furyl or thienyl group; R2 represents a straight chain or branched chain alkyl group of 1 to 6 carbon atoms; a cycloalkyl group of 4 to 8 carbon atoms unsubstituted or substituted with at least one lower alkyl group; a phenyl group unsubstituted or substituted with at least one lower alkyl group, a lower alkoxy group, a lower alkylthio group or a halogen atom; or a lower alkylthio group; R3 and R4 each represents a hydrogen atom or R2 and R3 or R2 and R4 when taken together represent an alkylene group of 2 to 5 carbon atoms unsubstituted or substituted with 1 or 2 lower alkyl groups; R5 represents a hydrogen atom or a lower alkyl group; and R6 represents a hydrogen atom, a lower alkyl group or an acyl group, and the pharmaceutically acceptable acid addition salt thereof having anti-inflammatory, analgesic, antipyretic, diuretic and hypotensive effects that can be used for preventing and curing diseases caused by inflammation, edema, hypertension, etc. are disclosed. Also disclosed is a process for preparing such derivative or a pharmaceutically acceptable acid addition salt thereof.