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2-(Acetyloxy)-5-iodobenzoic acid

Base Information Edit
  • Chemical Name:2-(Acetyloxy)-5-iodobenzoic acid
  • CAS No.:1503-54-4
  • Molecular Formula:C9H7 I O4
  • Molecular Weight:306.057
  • Hs Code.:2918990090
  • European Community (EC) Number:216-127-1
  • NSC Number:518712
  • UNII:Y952A6Q3L8
  • DSSTox Substance ID:DTXSID6074542
  • Nikkaji Number:J7.504C
  • Wikidata:Q82002855
  • Mol file:1503-54-4.mol
2-(Acetyloxy)-5-iodobenzoic acid

Synonyms:2-(Acetyloxy)-5-iodobenzoic acid;1503-54-4;O-Acetyl-5-iodosalicylic acid;2-acetyloxy-5-iodobenzoic acid;Benzoic acid, 2-(acetyloxy)-5-iodo-;5-Iodosalicylic acid acetate;5-Iodoacetylsalicylic acid;5-Iodo-2-acetoxybenzoic acid;AI3-15467;Salicylic acid, 5-iodo-, acetate;Y952A6Q3L8;EINECS 216-127-1;NSC-518712;Benzoic acid,2-(acetyloxy)-5-iodo-;5-Iodoaspirin;UNII-Y952A6Q3L8;SCHEMBL1319089;DTXSID6074542;C9-H7-I-O4;NSC518712;2-(Acetyloxy)-5-iodobenzoic acid #;NSC 518712

Suppliers and Price of 2-(Acetyloxy)-5-iodobenzoic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 7 raw suppliers
Chemical Property of 2-(Acetyloxy)-5-iodobenzoic acid Edit
Chemical Property:
  • Vapor Pressure:1E-06mmHg at 25°C 
  • Boiling Point:388.3°Cat760mmHg 
  • Flash Point:188.6°C 
  • PSA:63.60000 
  • Density:1.893g/cm3 
  • LogP:1.91470 
  • XLogP3:1.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:305.93891
  • Heavy Atom Count:14
  • Complexity:241
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)OC1=C(C=C(C=C1)I)C(=O)O
Technology Process of 2-(Acetyloxy)-5-iodobenzoic acid

There total 3 articles about 2-(Acetyloxy)-5-iodobenzoic acid 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:
Guidance literature:
Multi-step reaction with 2 steps
1: sulfuric acid / Diazotization.Eintragen der Diazoloesung in konzentrierte Jodwasserstoffsaeure und nachfolgendes Erwaermen auf 80-90grad
With sulfuric acid;
Guidance literature:
2-Hydroxy-5-jod-benzoesaeure, Acetanhydrid (2Mol), wenig konz. Schwefelsaeure, 50-60grad, 30Min.;
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