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10446-37-4

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10446-37-4 Usage

Description

4-METHOXY-2-(1-PHENYL-ETHYL)-PHENOL, also known as eugenol, is a chemical compound with the molecular formula C16H16O2. It is a colorless or pale yellow liquid with a strong, spicy aroma and is commonly found in essential oils such as clove oil. Eugenol possesses antibacterial, antifungal, and antioxidant properties, making it a versatile and important chemical compound with a wide range of industrial and pharmaceutical applications.

Uses

Used in Flavorings and Perfumes:
4-METHOXY-2-(1-PHENYL-ETHYL)-PHENOL is used as a flavoring agent for its strong, spicy aroma, and as a component in perfumes due to its distinctive scent.
Used in Traditional Medicine:
In traditional medicine, 4-METHOXY-2-(1-PHENYL-ETHYL)-PHENOL is used as an analgesic and anti-inflammatory agent, leveraging its natural pain-relieving and inflammation-reducing properties.
Used in Dentistry:
4-METHOXY-2-(1-PHENYL-ETHYL)-PHENOL is used as a local antiseptic and anesthetic in dentistry, thanks to its ability to kill bacteria and numb the area, making dental procedures more comfortable for patients.
Used in Industrial Applications:
In various industries, 4-METHOXY-2-(1-PHENYL-ETHYL)-PHENOL is used for its antibacterial, antifungal, and antioxidant properties, contributing to the preservation and enhancement of products in areas such as food, cosmetics, and pharmaceuticals.
Used in Pharmaceutical Applications:
4-METHOXY-2-(1-PHENYL-ETHYL)-PHENOL is utilized in the development of pharmaceutical products due to its therapeutic potential in treating various conditions, including its analgesic, anti-inflammatory, and antimicrobial effects.

Check Digit Verification of cas no

The CAS Registry Mumber 10446-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10446-37:
(7*1)+(6*0)+(5*4)+(4*4)+(3*6)+(2*3)+(1*7)=74
74 % 10 = 4
So 10446-37-4 is a valid CAS Registry Number.

10446-37-4SDS

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 4-methoxy-2-(1-phenylethyl)phenol

1.2 Other means of identification

Product number -
Other names 4-methoxy-2-(1-phenyl-ethyl)phenol

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:10446-37-4 SDS

10446-37-4Downstream Products

10446-37-4Relevant articles and documents

HBF4- and AgBF4-Catalyzed ortho-Alkylation of Diarylamines and Phenols

Rank, Christian K.,?zkaya, Bünyamin,Patureau, Frederic W.

supporting information, p. 6830 - 6834 (2019/09/12)

A silver-tetrafluoroborate- or HBF4-catalyzed ortho-alkylation reaction of phenols and diarylamines with styrenes has been explored. A broad substrate scope is presented as well as mechanistic experiments and discussion.

Dehydrative C-H alkylation and alkenylation of phenols with alcohols: Expedient synthesis for substituted phenols and benzofurans

Lee, Dong-Hwan,Kwon, Ki-Hyeok,Yi, Chae S.

supporting information; experimental part, p. 7325 - 7328 (2012/06/16)

A well-defined cationic Ru-H complex catalyzes the dehydrative C-H alkylation reaction of phenols with alcohols to form ortho-substituted phenol products. Benzofuran derivatives are efficiently synthesized from the dehydrative C-H alkenylation and annulation reaction of phenols with 1,2-diols. The catalytic C-H coupling method employs cheaply available phenols and alcohols, exhibits a broad substrate scope, tolerates carbonyl and amine functional groups, and liberates water as the only byproduct.

Efficient and general continuous-flow hydroarylation and hydroalkylation of styrenes

Rueping, Magnus,Bootwicha, Teerawut,Sugiono, Erli

experimental part, p. 2961 - 2965 (2011/02/22)

A simple and efficient continuous-flow hydroarylation of arenes and heteroarenes using various styrenes in conjunction with a heterogeneous catalyst has been developed. Additionally, this method has been successfully extended to the hydroalkylation of styrenes by employing 1,3-dicarbonyl compounds as the nucleophile. Multigram quantities of diarylmethanes have been prepared using this new flow method. Copyright

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