Welcome to LookChem.com Sign In|Join Free
  • or
2-(Cyclohex-1-en-1-yl)-1,3-dimethoxybenzene, commonly known as eugenol, is a naturally occurring phenylpropene compound that is found in a variety of plants, including clove, basil, and cinnamon. It is characterized by its distinctive, pleasant, spicy, and floral aroma, and is recognized for its diverse range of properties, such as analgesic, anti-inflammatory, and antimicrobial effects. Eugenol's versatility extends to its applications in various industries, from food and beverages to pharmaceuticals and cosmetics, where it is valued for its flavoring, fragrance, and therapeutic qualities.

27124-92-1

Post Buying Request

27124-92-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

27124-92-1 Usage

Uses

Used in Flavoring and Fragrance Industry:
Eugenol is used as a flavoring agent in food and beverages, capitalizing on its characteristic aromatic properties to enhance the sensory experience of these products. Its spicy and floral notes are particularly sought after in the creation of various culinary and beverage recipes.
Used in Perfumery and Essential Oils:
In the perfumery industry, eugenol is utilized for its ability to add depth and complexity to fragrances. Its spicy and floral scents contribute to the creation of unique and appealing perfume blends.
Used in Traditional Medicine and Dental Products:
Eugenol's analgesic, anti-inflammatory, and antimicrobial properties make it a popular ingredient in traditional medicine, where it is used to alleviate pain and reduce inflammation. In dental products, it is commonly found in temporary filling materials and as a component in certain dental cements due to its ability to numb the area and prevent bacterial growth.
Used in Pharmaceutical Industry:
Eugenol's potential antioxidant and anticancer effects have garnered interest in the pharmaceutical industry. It is being studied for its ability to combat oxidative stress and its potential to inhibit the growth of cancer cells, which could lead to the development of new therapeutic agents.
Used in Cosmetic Industry:
In the cosmetic industry, eugenol is employed for its antimicrobial and anti-inflammatory properties, which can be beneficial in skincare products for treating acne and other skin conditions. Its pleasant aroma also makes it a desirable ingredient in various cosmetic formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 27124-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,2 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27124-92:
(7*2)+(6*7)+(5*1)+(4*2)+(3*4)+(2*9)+(1*2)=101
101 % 10 = 1
So 27124-92-1 is a valid CAS Registry Number.

27124-92-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(cyclohexen-1-yl)-1,3-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 2-cyclohexenyl-1,3-dimethoxybenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:27124-92-1 SDS

27124-92-1Relevant academic research and scientific papers

Palladium-Catalysed Direct Cross-Coupling of Organolithium Reagents with Aryl and Vinyl Triflates

Vila, Carlos,Hornillos, Valentín,Giannerini, Massimo,Fa?anás-Mastral, Martín,Feringa, Ben L.

supporting information, p. 13078 - 13083 (2016/02/19)

A palladium-catalysed cross-coupling of organolithium reagents with aryl and vinyl triflates is presented. The reaction proceeds at 50 or 70 C with short reaction times, and the corresponding products are obtained with moderate to high yields, with a variety of alkyl and (hetero)aryl lithium reagents.

Arylalkene synthesis via decarboxylative cross-coupling of alkenyl halides

Tang, Jie,Goossen, Lukas J.

, p. 2664 - 2667 (2014/06/09)

A bimetallic catalyst system generated from readily available palladium(II) and copper(I) salts, 1,10-phenanthroline and tri-1-naphthylphosphine was found to efficiently mediate the decarboxylative cross-coupling of alkenyl bromides and chlorides with aromatic carboxylates. It allows the regiospecific synthesis of a broad range of aryl- and heteroarylalkenes in high yields.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 27124-92-1