17378-99-3

Basic information

• Product Name: 2-[2-(2-hydroxyethyl)phenyl]ethanol
• Synonyms: 2-[2-(2-hydroxyethyl)phenyl]ethanol;1,2-Benzenediethanol(9CI)
• CAS NO: 17378-99-3
• Molecular Formula: C₁₀H₁₄O₂
• Molecular Weight: 166.22
• Product Categories: PHENYL
• Mol File: 17378-99-3.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 303.2°Cat760mmHg
• Flash Point: 146°C
• Appearance: /
• Density: 1.107g/cm³
• Vapor Pressure: 0.000416mmHg at 25°C
• Refractive Index: 1.558
• CAS DataBase Reference: 2-[2-(2-hydroxyethyl)phenyl]ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[2-(2-hydroxyethyl)phenyl]ethanol(17378-99-3)
• EPA Substance Registry System: 2-[2-(2-hydroxyethyl)phenyl]ethanol(17378-99-3)

Safety Data

• Hazardous Substances Data: 17378-99-3(Hazardous Substances Data)

Usage

General Description

2-[2-(2-hydroxyethyl)phenyl]ethanol is a chemical compound with the molecular formula C14H18O2. It is an aromatic alcohol that contains a phenyl group and a hydroxyethyl group. This chemical is commonly used as a fragrance ingredient in perfumes and personal care products due to its pleasant aroma. It is also used as a solvent in various industrial applications. In addition, 2-[2-(2-hydroxyethyl)phenyl]ethanol is known for its antimicrobial and antibacterial properties, making it a common ingredient in antiseptic solutions and disinfectants. This chemical is considered to have low toxicity and is generally safe for use when handled properly.

InChI:InChI=1/C10H14O2/c11-7-5-9-3-1-2-4-10(9)6-8-12/h1-4,11-12H,5-8H2

Upstream product

• 7500-53-0 1,2-Phenylenediacetic acid 
• 613-73-0 1,2-phenylenediacetonitrile 
• 17532-66-0 ethyl 2-[2-(2-ethoxy-2-oxoethyl)phenyl]acetate 
• 19109-69-4 (o-Phenylen)bis(essigsaeure-methylester) 

Downstream Products

• 497157-41-2 2-{2-[2-(tert-butyldimethylsilanyloxy)-ethyl]-phenyl}-ethanol 
• 101098-50-4 1,2-bis-(2-dimethylamino-ethyl)-benzene 
• 34583-83-0 7-nitro-2,3,4,5-tetrahydro-1H-benzo[d]azepiney 
• 4424-20-8 2,3,4,5-tetrahydro-1H-3-benzazepine 
• 1022957-04-5 methanesulfonic acid 2-[2-(2-hydroxy-ethyl)-phenyl]-ethyl ester 
• 242-14-8 benzo[4,5]cyclohePt[1,2-b]indole 
• 411211-05-7 1,2-bis(2-cyanoethyl)benzene 
• 37949-03-4 5,6,8,9-tetrahydrobenzo[7]annulen-7-one 
• 112453-80-2 benzene-1,2-diethanethiol 
• 118636-00-3 1,2-bis-(2-diphenylphosphinoethyl)benzene 
• 130800-05-4 1,2-Bis(2'-iodoethyl)benzene 
• 136863-22-4 <2-(2-Hydroxyethyl)phenyl>essigsaeure 
• 121688-12-8 2(2-acetoxyethyl)phenylacetaldehyde 
• 497157-44-5 acetic acid 1-{2-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-benzyl}-allyl ester 

Relevant articles and documents

Compound as potassium channel modulator

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

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

(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