3-(2-ACETOXYPHENYL)-2-METHYL-1-PROPENE

Base Information

• Chemical Name: 3-(2-ACETOXYPHENYL)-2-METHYL-1-PROPENE
• CAS No.: 861009-82-7
• Molecular Formula: C12H14O2
• Molecular Weight: 190.242
• Hs Code.: 2915390090
• Mol file: 861009-82-7.mol

Synonyms:3-(2-ACETOXYPHENYL)-2-METHYL-1-PROPENE

Chemical Property of 3-(2-ACETOXYPHENYL)-2-METHYL-1-PROPENE

Chemical Property:

• Vapor Pressure: 0.00576mmHg at 25°C
• Boiling Point: 273.4°C at 760 mmHg
• Flash Point: 101.3°C
• PSA: 26.30000
• Density: 1.013g/cm³
• LogP: 2.73050

Purity/Quality:

97% ^*data from raw suppliers

3-(2-Acetoxyphenyl)-2-methyl-1-propene 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 3-(2-ACETOXYPHENYL)-2-METHYL-1-PROPENE

There total 3 articles about 3-(2-ACETOXYPHENYL)-2-METHYL-1-PROPENE 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:

phenol (108-95-2,27073-41-2) → acetic acid-(2-methallyl-phenyl ester) (861009-82-7)

Guidance literature:

Multi-step reaction with 3 steps

1: K₂CO₃; acetone

2: Erhitzen auf Siedetemperatur

With potassium carbonate; acetone;

DOI:10.1021/ja01305a044

Reference yield:

methylallyl phenyl ether (5820-22-4) → acetic acid-(2-methallyl-phenyl ester) (861009-82-7)

Guidance literature:

Multi-step reaction with 2 steps

1: Erhitzen auf Siedetemperatur

DOI:10.1021/ja01305a044 DOI:10.1021/jo01208a018

Reference yield:

acetic anhydride (108-24-7) + 2-(methylallyl)phenol (20944-88-1) → acetic acid-(2-methallyl-phenyl ester) (861009-82-7)

Guidance literature:

DOI:10.1021/ja01305a044 DOI:10.1021/jo01208a018

upstream raw materials:

acetic anhydride

2-(methylallyl)phenol

methylallyl phenyl ether

phenol

Downstream raw materials:

3-methylisochroman

hydrogen bromide

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