1-ALLYLOXYNAPHTHALENE

Base Information

• Chemical Name: 1-ALLYLOXYNAPHTHALENE
• CAS No.: 20009-25-0
• Molecular Formula: C13H12O
• Molecular Weight: 184.238
• Hs Code.: 2909309090
• Mol file: 20009-25-0.mol

Synonyms:Naphthalene,1-(2-propenyloxy)- (9CI);Naphthalene, 1-(allyloxy)- (6CI,7CI,8CI);1-(2-Propenyloxy)naphthalene;1-(Allyloxy)naphthalene;Allyl 1-naphthyl ether;Allyl a-naphthyl ether;a-Naphthol allyl ether;a-Naphthyl allyl ether;

Chemical Property of 1-ALLYLOXYNAPHTHALENE

Chemical Property:

• Vapor Pressure: 0.00128mmHg at 25°C
• Melting Point: -10 °C (decomp)
• Refractive Index: 1.595
• Boiling Point: 307.9 °C at 760 mmHg
• Flash Point: 120.2 °C
• PSA: 9.23000
• Density: 1.048 g/cm³
• LogP: 3.40460

Purity/Quality:

99% ^*data from raw suppliers

1-Allyloxynaphthalene ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 1-ALLYLOXYNAPHTHALENE

There total 13 articles about 1-ALLYLOXYNAPHTHALENE 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: 100.0%

α-naphthol (90-15-3) + allyl bromide (106-95-6) → allyl naphthyl ether (20009-25-0)

Guidance literature:

With potassium carbonate; In acetone; at 20 ℃; Reflux;

DOI:10.1021/ol901964z

Reference yield: 100.0%

allyl methyl carbonate (35466-83-2) + α-naphthol (90-15-3) → allyl naphthyl ether (20009-25-0)

Guidance literature:

With triphenylphosphine; palladium incarcerated copolymer; In tetrahydrofuran; Heating;

DOI:10.1021/ja029146j

Reference yield: 100.0%

1-Naphthyl allyl carbonate → allyl naphthyl ether (20009-25-0)

Guidance literature:

With diethyl malonate; 2,6-bis[4′-isopropyloxazolin-2′-yl]pyridine;

DOI:10.1002/(SICI)1521-3773(19991102)38:21<3163::AID-ANIE3163>3.0.CO;2-#

upstream raw materials:

α-naphthol

allyl bromide

sodium naphtholate

3-chloroprop-1-ene

Downstream raw materials:

3-(1-naphthyloxy)propane-1,2-diol

α-naphthol

2-allyl-1-naphthol

(S)-1-isopropylamino-3-(1-naphthyloxy)-2-propanol

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