Phenyl acetylsalicylate

Base Information

• Chemical Name: Phenyl acetylsalicylate
• CAS No.: 134-55-4
• Molecular Formula: C15H12 O4
• Molecular Weight: 256.258
• Hs Code.: 2918229000
• European Community (EC) Number: 205-147-6
• NSC Number: 97356
• UNII: 7QP16N8ZNA
• DSSTox Substance ID: DTXSID20870484
• Nikkaji Number: J5.597B
• Wikidata: Q27268724
• ChEMBL ID: CHEMBL163612
• Mol file: 134-55-4.mol

Synonyms:Phenyl acetylsalicylate;Spiroform;Acetylsalol;Phennin;Vesipyrin;134-55-4;Phenyl O-acetylsalicylate;phenyl 2-acetyloxybenzoate;Acetylphenylsalicylate;phenyl 2-(acetyloxy)benzoate;Salicylic acid acetate, phenyl ester;7QP16N8ZNA;aspirin phenyl ester;NSC-97356;Phenylacetylsalicylate;PHENYLASPIRINATE;phenyl 2-acetoxybenzoate;UNII-7QP16N8ZNA;SCHEMBL25954;CHEMBL163612;DTXSID20870484;CHEBI:135050;NSC97356;2-Acetoxy-benzoic acid phenyl ester;EINECS 205-147-6;PHENYL ACETYLSALICYLATE [MI];NSC 97356;CCG-286410;AF-399/33198054;Q27268724

Chemical Property of Phenyl acetylsalicylate

Chemical Property:

• Vapor Pressure: 1.46E-06mmHg at 25°C
• Melting Point: 97°
• Refractive Index: 1.4872 (estimate)
• Boiling Point: 398.6°Cat760mmHg
• Flash Point: 202°C
• PSA: 52.60000
• Density: 1.217g/cm³
• LogP: 2.83110
• Water Solubility.: 20mg/L(21 oC)
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 256.07355886
• Heavy Atom Count: 19
• Complexity: 320

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OC1=CC=CC=C1C(=O)OC2=CC=CC=C2

Technology Process of Phenyl acetylsalicylate

There total 6 articles about Phenyl acetylsalicylate 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: 88.0%

aspirin (50-78-2,98201-60-6) + phenylboronic acid (98-80-6) → phenyl 2-acetoxybenzoate (134-55-4)

Guidance literature:

With copper(II) bis(trifluoromethanesulfonate); urea; In ethyl acetate; at 60 ℃; for 12h;

DOI:10.1021/jo101558s

Reference yield:

acetic anhydride (108-24-7) + phenyl Salicylate (118-55-8) → phenyl 2-acetoxybenzoate (134-55-4)

Guidance literature:

Reference yield:

phenyl Salicylate (118-55-8) + acetyl chloride (75-36-5) → phenyl 2-acetoxybenzoate (134-55-4)

Guidance literature:

upstream raw materials:

acetic anhydride

phenyl Salicylate

acetyl chloride

phenyltrimethylsilyl ether

Downstream raw materials:

2,2'-dihydroxybenzophenone

5-acetylsalicylic acid

2-hydroxy-3,5-dinitro-benzoic acid-(4-nitro-phenyl ester)

2-hydroxy-3,5-dinitro-benzoic acid phenyl ester

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
  FOB CIF CFR EXW
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 134-55-4 phenyl O-acetylsalicylate

Send

Send

Metric Ton KG G Pound L ML

Send

Send