30595-80-3

Usage

Uses

Used in Fragrance Industry:
2-(2,6-dimethylphenyl)ethanol is used as a fragrance ingredient for its floral scent, contributing to the development of perfumes, soaps, and other personal care products. Its appealing aroma enhances the sensory experience of these products, making them more attractive to consumers.
Used in Food Industry:
In the food industry, 2-(2,6-dimethylphenyl)ethanol serves as a flavoring agent, adding unique taste profiles to food products. Its ability to impart distinct flavors makes it a valuable component in the creation of various food items, enhancing their overall flavor profiles.
Used in Antiseptic Products:
Leveraging its antimicrobial properties, 2-(2,6-dimethylphenyl)ethanol is utilized in some antiseptic products. It helps to inhibit the growth of harmful microorganisms, providing a layer of protection against potential infections and contributing to the maintenance of hygiene and cleanliness.
It is crucial to handle 2-(2,6-dimethylphenyl)ethanol with care due to its potential hazards. Ingestion, inhalation, and skin or eye contact can cause harm or irritation. Proper safety measures should be taken to ensure the safe use of this chemical compound in various applications.

InChI:InChI=1/C10H14O/c1-8-4-3-5-9(2)10(8)6-7-11/h3-5,11H,6-7H2,1-2H3

Upstream product

• 87-62-7 2,6-dimethylaniline 
• 75-21-8 oxirane 
• 576-22-7 2-Bromo-m-xylene 
• 74-96-4 ethyl bromide 
• 19819-98-8 2-o-tolylethanol 
• 103839-06-1 3,4-dihydro-5-methyl-2(1H)-benzopyran 
• 245041-48-9 2-chloromethyl-6-methylphenethyl acetate 

Downstream Products

• 30595-81-4 2-(2-chloroethyl)-1,3-dimethylbenzene 
• 131750-31-7 2-(2',6'-dimethylphenyl)-ethanoacetate 
• 65848-79-5 methyl 2-(2,6-dimethylphenyl)ethyl ether 
• 79927-86-9 2,6-dimethyl-β-phenethyl bromide 
• 46398-51-0 C₁₁H₁₈N₄ 
• 30953-60-7 2,6-Dimethylphenethylhydrazin 
• 131750-33-9 3-<4-(acetoxyethyl)-3,5-dimethylphenyl>-1-chloro-3-oxopropane 
• 131750-32-8 3-<3-(acetoxyethyl)-2,4-dimethylphenyl>-1-chloro-3-oxopropane 

Relevant academic research and scientific papers

PROCESS FOR PREPARING SUBSTITUTED 2-ARYLETHANOLS

The invention relates to a process for preparing substituted 2-arylethanols of the formula (I) by reacting Grignard compounds of the formula (II) in the presence of a copper compound with ethylene oxide. Moreover, the invention relates to novel substituted 2-arylethanols of the formula (I).

Synthesis and Biological Evaluation of Fentanyl Analogues Modified at Phenyl Groups with Alkyls

A series of fentanyl analogues modified at the phenyl group of the phenethyl with alkyl and/or hydroxyl and alkoxy, and the phenyl group in the anilido moiety replaced with benzyl or substituted benzyl, were synthesized. The in vitro opioid receptor functional activity of these compounds was evaluated by assessment of their ability to modulate forskolin-stimulated cAMP accumulation and by their ability to induce β-arrestin2 recruitment. Compound 12 is a potent μ-opioid (MOP) receptor agonist, a potent κ-opioid (KOP) receptor antagonist with weak β-arrestin2 recruitment activity. Compounds 10 and 11 are potent MOP receptor agonists with weak δ-opioid (DOP) receptor antagonist activity and moderate KOP receptor antagonist activity as well as weak β-arrestin2 recruitment activity at the MOP receptor. These compounds are promising leads for discovery of potent opioid analgesics with reduced side effects relative to clinically available strong opioid analgesics.

Fentanyl analogue and application thereof

The invention discloses a fentanyl analogue and application thereof. A general structural formula of a compound is as follows (described in the following description), wherein R1 is a hydrogen group,a methyl group, a hydroxyl group, a methoxyl group, a halogen and a cyano group, and R2 is a phenyl group, a benzyl group and 3,5-benzyldimethyl. The compound provided by the invention embodies the activating effect of a mu-opioid receptor and the recruitment function of weak beta-arrestin 2, and therefore, the compound can be used as an analgesic drug and can overcome the respiration inhibition effect caused by activating a beta-arrestin 2 signal pathway.

Synthesis and antispasmodic activity of nature identical substituted indanes and analogues

The synthesis of a series of substituted indanes which provide routes to nature-identical compounds and their analogues is reported. The smooth muscle relaxant activity of a series of substituted indanes and indanones together with their analogues has been measured. A compound with significant smooth muscle relaxant activity has been identified.