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2-Methoxybenzoic anhydride

Base Information
  • Chemical Name:2-Methoxybenzoic anhydride
  • CAS No.:64508-50-5
  • Molecular Formula:C16H14 O5
  • Molecular Weight:286.284
  • Hs Code.:2918990090
  • European Community (EC) Number:800-981-2
  • DSSTox Substance ID:DTXSID70574647
  • Nikkaji Number:J587.277D
  • Wikidata:Q82463777
  • Mol file:64508-50-5.mol
2-Methoxybenzoic anhydride

Synonyms:2-methoxybenzoic anhydride;64508-50-5;(2-Methoxybenzoyl) 2-methoxybenzoate;SCHEMBL446339;2-methoxybenzoic acid anhydride;DTXSID70574647;CPPYQMZQDONVGK-UHFFFAOYSA-N;(2-Methoxybenzoyl)2-methoxybenzoate;AKOS025396895

Suppliers and Price of 2-Methoxybenzoic anhydride
Supply Marketing:
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
  • American Custom Chemicals Corporation
  • 2-METHOXY BENZOIC ANHYDRIDE 95.00%
  • 5MG
  • $ 501.05
Total 4 raw suppliers
Chemical Property of 2-Methoxybenzoic anhydride
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:72.4 °C 
  • Refractive Index:1.564 
  • Boiling Point:453.504°C at 760 mmHg 
  • Flash Point:202.335°C 
  • PSA:61.83000 
  • Density:1.22g/cm3 
  • LogP:2.70100 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:286.08412354
  • Heavy Atom Count:21
  • Complexity:334
Purity/Quality:

97% *data from raw suppliers

2-METHOXY BENZOIC ANHYDRIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC=CC=C1C(=O)OC(=O)C2=CC=CC=C2OC
Technology Process of 2-Methoxybenzoic anhydride

There total 11 articles about 2-Methoxybenzoic anhydride 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:
With iodine; triethylamine; triphenylphosphine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/j.tetlet.2015.12.009
Guidance literature:
With 1,3-bis-(diphenylphosphino)propane; water; palladium diacetate; triethylamine; In N,N-dimethyl-formamide; at 20 - 115 ℃; for 6h; under 760.051 Torr; Inert atmosphere; Autoclave;
DOI:10.1039/c2cc16611a
Guidance literature:
With tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide; In decane; acetonitrile; at 70 ℃; for 0.5h; Green chemistry;
DOI:10.1016/j.tetlet.2016.02.036
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