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Methyl 3,5-diiodobenzoate

Base Information Edit
  • Chemical Name:Methyl 3,5-diiodobenzoate
  • CAS No.:14266-19-4
  • Molecular Formula:C8H6 I2 O2
  • Molecular Weight:387.943
  • Hs Code.:2916399090
  • European Community (EC) Number:604-303-4
  • DSSTox Substance ID:DTXSID80700753
  • Wikidata:Q82632214
  • Mol file:14266-19-4.mol
Methyl 3,5-diiodobenzoate

Synonyms:METHYL 3,5-DIIODOBENZOATE;14266-19-4;3,5-DIIODOBENZOIC ACID METHYL ESTER;Methyl3,5-diiodobenzoate;SCHEMBL231885;DTXSID80700753;YYSITUQNFNKVLR-UHFFFAOYSA-N;AKOS017547783;EN300-255598

Suppliers and Price of Methyl 3,5-diiodobenzoate
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
  • TRC
  • Methyl3,5-Diiodobenzoate
  • 100mg
  • $ 330.00
  • American Custom Chemicals Corporation
  • 3,5-DIIODOBENZOIC ACID METHYL ESTER 95.00%
  • 5MG
  • $ 496.95
Total 2 raw suppliers
Chemical Property of Methyl 3,5-diiodobenzoate Edit
Chemical Property:
  • Refractive Index:1.667 
  • PSA:26.30000 
  • LogP:2.68240 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:387.84572
  • Heavy Atom Count:12
  • Complexity:162
Purity/Quality:

97% *data from raw suppliers

Methyl3,5-Diiodobenzoate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC(=O)C1=CC(=CC(=C1)I)I
Technology Process of Methyl 3,5-diiodobenzoate

There total 8 articles about Methyl 3,5-diiodobenzoate 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 potassium carbonate; In acetone; at 56 ℃; for 12h;
DOI:10.1002/cplu.201500104
Guidance literature:
With tetrahydrofuran; isopentyl nitrite;
DOI:10.1021/ja9812047
Guidance literature:
With sulfuric acid; for 7.5h; Reflux;
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