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2-Methoxy-5-(prop-2-en-1-yl)phenol, also known as eugenol, is a naturally occurring organic compound found in the essential oils of plants like cloves, cinnamon, and bay leaves. It is a colorless to pale yellow oily liquid with a characteristic spicy, sweet odor. This phenolic compound has a molecular formula of C10H12O2 and a molecular weight of 164.20 g/mol. Eugenol is widely used in the food, pharmaceutical, and flavoring industries due to its antimicrobial, anti-inflammatory, and analgesic properties. It is also known for its potential applications in dentistry as an antiseptic and local anesthetic. The compound's chemical structure consists of a phenol group with a methoxy group at the 2-position and an allyl group at the 5-position, which contributes to its unique properties and applications.

1941-09-9

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1941-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1941-09-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1941-09:
(6*1)+(5*9)+(4*4)+(3*1)+(2*0)+(1*9)=79
79 % 10 = 9
So 1941-09-9 is a valid CAS Registry Number.

1941-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetoxy-4-allyl-1-methoxy-benzene

1.2 Other means of identification

Product number -
Other names Chavibetolacetat

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:1941-09-9 SDS

1941-09-9Relevant academic research and scientific papers

Structure–activity relationships and docking studies of hydroxychavicol and its analogs as xanthine oxidase inhibitors

Nishiwaki, Keiji,Ohigashi, Kanae,Deguchi, Takahiro,Murata, Kazuya,Nakamura, Shinya,Matsuda, Hideaki,Nakanishi, Isao

, p. 741 - 747 (2018/07/05)

Hydroxychavicol (HC), which is obtained from the leaves of Piper betle LINN. (Piperaceae), inhibits xanthine oxidase (XO) with an IC50 value of 16.7μM, making it more potent than the clinically used allopurinol (IC50=30.7μM). Herein, a structure–activity relationship analysis of the polar part analogs of HC was conducted and an inhibitor was discovered with a potency 13 times that of HC. Kinetic studies have revealed that HC and its active analog inhibit XO in an uncompetitive manner. The binding structure prediction of these inhibitor molecules to the XO complex with xanthine suggested that both compounds (HC and its analog) could simultaneously form hydrogen bonds with xanthine and XO.

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