Potassium phenylacetate

Base Information

• Chemical Name: Potassium phenylacetate
• CAS No.: 13005-36-2
• Molecular Formula: C8H7KO2
• Molecular Weight: 174.241
• Hs Code.: 2916340090
• Mol file: 13005-36-2.mol

Synonyms:Aceticacid, phenyl-, potassium salt (8CI);Benzeneacetic acid, potassium salt (9CI);

Chemical Property of Potassium phenylacetate

Chemical Property:

• Appearance/Colour: White powder
• Vapor Pressure: 0.001Pa at 25℃
• Melting Point: 76.5ºC
• Boiling Point: 265.5 °C at 760 mmHg
• Flash Point: 156.2 °C
• PSA: 40.13000
• Density: 1.257g/cm3
• LogP: -0.02100

Purity/Quality:

99% ^*data from raw suppliers

PotassiumPhenylacetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Potassium phenylacetate

There total 6 articles about Potassium phenylacetate 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: 95.0%

benzeneacetic acid methyl ester (101-41-7) → potassium phenylacetate (13005-36-2)

Guidance literature:

With potassium tert-butylate; water; In ethanol; at 60 ℃;

DOI:10.1021/ja107103b

Reference yield: 94.0%

PdCl2 (PPH3)2 + benzyl chloride (100-44-7) → potassium phenylacetate (13005-36-2)

Guidance literature:

With potassium hydroxide; triphenylphosphine; In methanol;

Reference yield: 86.0%

→ potassium phenylacetate (13005-36-2)

Guidance literature:

upstream raw materials:

benzyl chloride

benzeneacetic acid methyl ester

phenylacetic acid

Ethyl 2-phenylethanoate

Downstream raw materials:

benzeneacetic acid methyl ester

phenylacetic anhydride

Phenyl-acetic acid [(3-chloro-phenyl)-isopropoxycarbonyl-amino]-methyl ester

Phenyl-acetic acid (isopropoxycarbonyl-phenyl-amino)-methyl ester