17378-99-3 Usage
Description
2-[2-(2-hydroxyethyl)phenyl]ethanol is an aromatic alcohol with the molecular formula C14H18O2. It features a phenyl group and a hydroxyethyl group, contributing to its unique chemical properties and applications.
Uses
Used in Fragrance Industry:
2-[2-(2-hydroxyethyl)phenyl]ethanol is used as a fragrance ingredient for its pleasant aroma, enhancing the scent profiles of perfumes and personal care products.
Used in Industrial Applications:
This chemical compound serves as a solvent in various industrial processes, leveraging its ability to dissolve other substances effectively.
Used in Antiseptic and Disinfectant Products:
2-[2-(2-hydroxyethyl)phenyl]ethanol is utilized as an antimicrobial and antibacterial agent in antiseptic solutions and disinfectants, helping to prevent the spread of infections and maintain cleanliness.
Given its low toxicity and general safety when handled properly, 2-[2-(2-hydroxyethyl)phenyl]ethanol is a versatile chemical with applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17378-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,7 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17378-99:
(7*1)+(6*7)+(5*3)+(4*7)+(3*8)+(2*9)+(1*9)=143
143 % 10 = 3
So 17378-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2/c11-7-5-9-3-1-2-4-10(9)6-8-12/h1-4,11-12H,5-8H2
17378-99-3Relevant articles and documents
Compound as potassium channel modulator
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Paragraph 0606; 0608; 0609; 0610, (2018/07/30)
The invention relates to a compound as a potassium channel modulator, which is a compound of a formula (I) or a pharmaceutically acceptable salt thereof. The compound or the pharmaceutically acceptable salt thereof is effective for curing and preventing diseases and symptoms influenced by the activity of potassium ion channels.
Synthesis of 3-substituted tetrahydrofuran and 4-substituted tetrahydropyran derivatives by cyclization of dicarboxylic acids with InBr 3/TMDS
Pehlivan, Leyla,Metay, Estelle,Delbrayelle, Dominique,Mignani, Gerard,Lemaire, Marc
supporting information; experimental part, p. 4689 - 4693 (2012/09/22)
An efficient reduction followed by cyclization of diacid compounds with the InBr3/TMDS system is reported. This system allows the formation of five- and six-membered ring ethers substituted in the 3- or 4-position. Copyright
Application of the B-alkyl Suzuki-Miyaura cross-coupling reaction to the stereoselective synthesis of analogues of (3S)-oxidosqualene
Winne, Johan M.,Guang, Bing,D'Herde, Jo,De Clercq, Pierre J.
, p. 4815 - 4818 (2007/10/03)
(Chemical Equation Presented) A general method is described for the direct and stereoselective synthesis of epoxypolyenes via Suzuki-Miyaura cross-coupling reaction of 1-iodoalkenes with B-alkylboron compounds. It allows for the straightforward and conver