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.
10446-37-4Relevant 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
