2-Allyl-4-ethoxyphenol

Base Information

• Chemical Name: 2-Allyl-4-ethoxyphenol
• CAS No.: 142875-24-9
• Molecular Formula: C11H14 O2
• Molecular Weight: 178.23
• Hs Code.: 2909500000
• DSSTox Substance ID: DTXSID60366538
• Nikkaji Number: J2.222.659B
• Wikidata: Q82151795
• ChEMBL ID: CHEMBL2271181
• Mol file: 142875-24-9.mol

Synonyms:2-allyl-4-ethoxyphenol;142875-24-9;4-ethoxy-2-(prop-2-en-1-yl)phenol;4-ethoxy-2-prop-2-enylphenol;SCHEMBL9614914;CHEMBL2271181;DTXSID60366538;AKOS008967674;EN300-09347;Z56979391

Chemical Property of 2-Allyl-4-ethoxyphenol

Chemical Property:

• Vapor Pressure: 0.00117mmHg at 25°C
• Boiling Point: 290.6°Cat760mmHg
• Flash Point: 137.4°C
• PSA: 29.46000
• Density: 1.031g/cm³
• LogP: 2.51940
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 178.099379685
• Heavy Atom Count: 13
• Complexity: 156

Purity/Quality:

96% ^*data from raw suppliers

4-ethoxy-2-(prop-2-en-1-yl)phenol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC1=CC(=C(C=C1)O)CC=C

Technology Process of 2-Allyl-4-ethoxyphenol

There total 5 articles about 2-Allyl-4-ethoxyphenol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(1-(allyloxy)-4-ethoxybenzene) (100058-51-3) → 2-allyl-4-ethoxyphenol (142875-24-9)

Guidance literature:

With N,N-diethylaniline;

DOI:10.1021/ja01235a006

Reference yield:

4-Ethoxyphenol (622-62-8) → 2-allyl-4-ethoxyphenol (142875-24-9)

Guidance literature:

Multi-step reaction with 2 steps

1: K₂CO₃; acetone

2: N_.N-diethyl-aniline

With potassium carbonate; acetone; N,N-diethylaniline;

DOI:10.1021/ja01235a006

Reference yield:

hydroquinone (123-31-9,8027-02-9) → 2-allyl-4-ethoxyphenol (142875-24-9)

Guidance literature:

Multi-step reaction with 3 steps

1: ethanolic KOH

2: K₂CO₃; acetone

3: N_.N-diethyl-aniline

With potassium hydroxide; potassium carbonate; acetone; N,N-diethylaniline;

DOI:10.1021/ja01235a006

upstream raw materials:

diphenylether

(1-(allyloxy)-4-ethoxybenzene)

N,N-diethylaniline

4-Ethoxyphenol

Downstream raw materials:

1-acetoxy-4-ethoxy-2-allyl-benzene

Refernces

• 1、 Plettner, Erika,Gries, Regine. "Agonists and antagonists of antennal responses of gypsy moth (Lymantria dispar) to the pheromone (+)-disparlure and other odorants". body text. p. 3708 - 3719. Retrieved 2011/07/30.