136911-16-5

Basic information

• Product Name: Benzenemethanol, 3-methoxy-2-(2-propenyl)-
• CAS NO: 136911-16-5
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 136911-16-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 3-methoxy-2-(2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 3-methoxy-2-(2-propenyl)-(136911-16-5)
• EPA Substance Registry System: Benzenemethanol, 3-methoxy-2-(2-propenyl)-(136911-16-5)

Safety Data

• Hazardous Substances Data: 136911-16-5(Hazardous Substances Data)

Usage

Description

Benzenemethanol, 3-methoxy-2-(2-propenyl)-, also known as eugenol, is a naturally occurring compound found in cloves, nutmeg, and cinnamon. It is a colorless to pale yellow liquid with a strong, spicy odor and taste. Eugenol possesses antimicrobial, antioxidant, and analgesic properties, making it a valuable compound in traditional medicine and natural health products. It is also commonly used as a flavoring agent in food and beverages, as well as in the fragrance and pharmaceutical industries. Eugenol has been studied for its potential anti-inflammatory and anti-cancer effects, showing promising results in preliminary research.

Uses

Used in Flavor and Fragrance Industry:
Benzenemethanol, 3-methoxy-2-(2-propenyl)is used as a flavoring agent for its strong, spicy odor and taste in food and beverages, enhancing the sensory experience of these products.
Used in Pharmaceutical Industry:
Benzenemethanol, 3-methoxy-2-(2-propenyl)is used as an active ingredient in traditional medicine and natural health products due to its antimicrobial, antioxidant, and analgesic properties, contributing to the treatment and management of various health conditions.
Used in Antimicrobial Applications:
Benzenemethanol, 3-methoxy-2-(2-propenyl)is used as an antimicrobial agent for its ability to inhibit the growth of harmful microorganisms, making it suitable for use in various medical and hygiene-related applications.
Used in Antioxidant Applications:
Benzenemethanol, 3-methoxy-2-(2-propenyl)is used as an antioxidant to protect against oxidative stress and damage, which can contribute to the prevention of various diseases and the maintenance of overall health.
Used in Analgesic Applications:
Benzenemethanol, 3-methoxy-2-(2-propenyl)is used as an analgesic agent for its pain-relieving properties, providing relief from various types of pain and discomfort.
Used in Anti-inflammatory Applications:
Benzenemethanol, 3-methoxy-2-(2-propenyl)is used as an anti-inflammatory agent for its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Anti-cancer Applications:
Benzenemethanol, 3-methoxy-2-(2-propenyl)is used as a potential anti-cancer agent, showing promising results in preliminary research for its ability to inhibit tumor growth and progression. Further studies are needed to fully understand its potential applications in cancer treatment.

Upstream product

• 1613271-10-5 2-allyl-3-methoxybenzyl 3,5-dinitrobenzoate 
• 153974-48-2 3-methoxy-O-tert-butyldimethylsilylbenzyl alcohol 
• 6971-51-3 3-methoxybenzyl alcohol 
• 223734-55-2 2-allyl-3-methoxy-O-tert-butyldimethylsilylbenzyl alcohol 
• 106-95-6 allyl bromide 

Downstream Products

• 94956-98-6 2-allyl-3-methoxybenzaldehyde 
• 81846-19-7 treprostinil 
• 101692-02-8 (1R,2R,3aS,9aS)-2,3,3a,4,9,9a-hexahydro-1-((S)-3-hydroxyoctyl)-1H-cyclopenta[b]naphthalene-2,5-diol 
• 223734-57-4 (6S)-1-[3-methoxy-2-(2-propenyl)phenyl]-6-[(tetrahydro-2H-pyran-2-yl)oxy]-2-undecyn-1-one 
• 223734-56-3 3-methoxy-2-(2-propenyl)-α-[(5S)-5-[(tetrahydro-2H-pyran-2-yl)oxy]-1-decynyl]benzenemethanol 
• 223734-58-5 (αS)-3-methoxy-2-(2-propenyl)-α-[(5S)-5-[(tetrahydro-2H-pyran-2-yl)oxy]-1-decynyl]benzenemethanol 
• 223734-59-6 (1,1-dimethylethyl)[[(1S,6S)-1-[3-methoxy-2-(2-propenyl)phenyl]-6-[(tetrahydro-2H-pyran-2-yl)oxy]-2-undecynyl]oxy]dimethylsilane 
• 1613271-12-7 (R)-1-(2-allyl-3-methoxyphenyl)-6,7-bis((tert-butyldimethylsilyl)oxy)hept-2-yn-1-one 
• 1613271-13-8 (1S,6R)-1-(2-allyl-3-methoxyphenyl)-6,7-bis((tert-butyldimethylsilyl)oxy)hept-2-yn-1-ol 
• 1613271-14-9 (5S,10R)-5-(2-allyl-3-methoxyphenyl)-10-((tert-butyldimethylsilyl)oxy)-2,2,3,3,13,13,14,14-octamethyl-4,12-dioxa-3,13-disilapentadec-6-yne 
• 1613271-10-5 2-allyl-3-methoxybenzyl 3,5-dinitrobenzoate 
• 136911-17-6 o-(chloromethyl)-2-allylanisole 

Relevant articles and documents

AMINE SALTS OF A PROSTACYCLIN ANALOG

The present invention provides amine salts of the prostacyclin analogue of Formula I and processes for generating these amine salts.

1-(PIPERIDIN-4-YL)-1H-INDOLE DERIVATIVE

The present invention provides a compound represented by the formula (1) or a pharmacologically acceptable salt thereof, or a hydrate thereof (provided that a compound in which all of R4a, R4b, and R4c are hydrogen atoms is excluded.): [wherein R1 represents a hydrogen atom, R2 represents a hydrogen atom, R3 represents the formula: wherein R4a, R4b, and R4c are the same as or different from each other and each represents a hydrogen atom, a C1-6 alkyl group or a C1-6 alkoxy group, etc.]

Palladium-catalyzed carbonylative cyclization via trapping of acylpalladium derivatives with internal enolates. Its scope and factors affecting the C-to-O ratio

The Pd-catalyzed carbonylative cyclization reaction involving ω-acyl-substituted acylpalladium derivatives can proceed via intramolecular trapping with either C- or O-enolates; the preferential formation of either 5- or 6-membered rings dictates the C-to-