Furfuryl salicylate

Base Information

Chemical Name:Furfuryl salicylate
CAS No.:25485-89-6
Molecular Formula:C₁₂H₁₀O₄
Molecular Weight:218.209
Hs Code.:
DSSTox Substance ID:DTXSID50180169
Nikkaji Number:J48.322B
Wikidata:Q83050686
Mol file:25485-89-6.mol

Synonyms:Furfuryl salicylate;furan-2-ylmethyl 2-hydroxybenzoate;25485-89-6;Furfuryl alcohol, salicylate;S 16;Salicylic acid, furfuryl ester;Salicylic acid, 2-furfuryl ester;Benzoic acid, 2-hydroxy-, 2-furanylmethyl ester;Benzoic acid, 2-hydroxy-, 2-furanylmethyl ester (9CI);SCHEMBL17010758;DTXSID50180169;S-16;LS-144333

Suppliers and Price of Furfuryl salicylate

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

Total 5 raw suppliers

Chemical Property of Furfuryl salicylate

Chemical Property:

Vapor Pressure:0.000127mmHg at 25°C
Boiling Point:324.8°C at 760 mmHg
Flash Point:150.2°C
PSA：59.67000
Density:1.289g/cm³
LogP:2.34220
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:218.05790880
Heavy Atom Count:16
Complexity:241

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)OCC2=CC=CO2)O

Technology Process of Furfuryl salicylate

There total 1 articles about Furfuryl salicylate 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: 70.0%

: 98-00-0,25212-86-6,93793-62-5
(2-furyl)methyl alcohol

: 69-72-7,25496-36-0,8052-31-1
salicylic acid

: 25485-89-6
C₁₂H₁₀O₄

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 0 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.tet.2016.02.032

Reference yield:

: 25485-89-6
C₁₂H₁₀O₄

: C₂₄H₂₁NO₅

: C₂₄H₂₁NO₅

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 30 °C / Inert atmosphere

2: potassium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 30 °C / Inert atmosphere

3: dirhodium tetraacetate / dichloromethane / 25 °C / Inert atmosphere

With dirhodium tetraacetate; tetra-(n-butyl)ammonium iodide; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2016.02.032

Reference yield:

: 25485-89-6
C₁₂H₁₀O₄

: C₂₉H₃₁N₃O₅

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 30 °C / Inert atmosphere

2: potassium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 30 °C / Inert atmosphere

With tetra-(n-butyl)ammonium iodide; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2016.02.032