4799-66-0

Basic information

• Product Name: ETHANOL,2-(ALPHA-METHYLBENZYLOXY)-
• Synonyms: ETHANOL,2-(ALPHA-METHYLBENZYLOXY)-;4-PHENYL-3-OXAPENTANOL;2-(1-Phenylethoxy)ethanol;2-(α-Methylbenzyloxy)ethanol
• CAS NO: 4799-66-0
• Molecular Formula: C₁₀H₁₄O₂
• Molecular Weight: 166.217
• Mol File: 4799-66-0.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 257.5°Cat760mmHg
• Flash Point: 103.8°C
• Appearance: /
• Density: 1.039g/cm³
• Vapor Pressure: 0.00742mmHg at 25°C
• Refractive Index: 1.516
• CAS DataBase Reference: ETHANOL,2-(ALPHA-METHYLBENZYLOXY)-(CAS DataBase Reference)
• NIST Chemistry Reference: ETHANOL,2-(ALPHA-METHYLBENZYLOXY)-(4799-66-0)
• EPA Substance Registry System: ETHANOL,2-(ALPHA-METHYLBENZYLOXY)-(4799-66-0)

Safety Data

• Hazardous Substances Data: 4799-66-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H14O2/c1-9(12-8-7-11)10-5-3-2-4-6-10/h2-6,9,11H,7-8H2,1H3

Upstream product

• 100-42-5 styrene 
• 107-21-1 ethylene glycol 
• 1517-69-7 (R)-1-phenylethanol 
• 585-71-7 (1-bromoethyl)benzne 
• 98-85-1 1-Phenylethanol 
• 936-51-6 2-phenyl-1,3-dioxolane 
• 917-54-4 methyllithium 
• 3674-77-9 2-methyl-2-phenyl-1,3-dioxolane 
• 75-21-8 oxirane 

Downstream Products

• 78759-31-6 1,2-bis-(1-phenyl-ethoxy)-ethane 

Relevant articles and documents

Catalytic hydroalkoxylation of alkenes by iron(III) catalyst

Catalytic hydroalkoxylation of alkenes by iron(III) chloride in the presence of toluenesulfonic acid (TsOH) was developed in moderate to good yields up to 91%. Intramolecular cyclization of 5-hydroxyl pentene afforded 2-methyltetrahedronfuran in 63% yield.

Effective Au(III)-CuCl2-catalyzed addition of alcohols to alkenes

Alkenes can be activated by Au(III) catalysts, and the effective addition of alcohols to alkenes can be carried out under mild conditions with Au(III), provided that catalytic amounts of CuCl2 are added, which significantly stabilize the cationic Au(III). The Royal Society of Chemistry.

9-(2-Aryloxyethyl) derivatives of adenine - A new class of non-nucleosidic antiviral agents

New 9-(aryloxyalkyl) derivatives of adenine have been prepared by alkylation of adenine with tosylates, bromides, and α-chloro ethers containing terminal aromatic fragments in anhydrous DMF in the presence of potassium carbonate. The compounds of the 9-(2-phenoxyethyl)adenine series appear to be highly reactive against cytomegaloviruses of mankind in vitro, while derivatives of 9-(2-benzyloxyethyl)adenine demonstrate anti-HIV-1 activity. Compounds with shorter or longer chains, and also compounds which do not have aromatic fragments at the ends of the chains, do not possess antiviral activity.