5-Benzoyl-2-furancarboxaldehyde

Base Information

Chemical Name:5-Benzoyl-2-furancarboxaldehyde
CAS No.:13529-18-5
Molecular Formula:C12H8O3
Molecular Weight:200.194
Hs Code.:
DSSTox Substance ID:DTXSID601305021
Nikkaji Number:J2.351.050B
Mol file:13529-18-5.mol

Synonyms:13529-18-5;5-Benzoyl-2-furancarboxaldehyde;SCHEMBL11297255;DTXSID601305021

Suppliers and Price of 5-Benzoyl-2-furancarboxaldehyde

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 0 raw suppliers

Chemical Property of 5-Benzoyl-2-furancarboxaldehyde

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:200.047344113
Heavy Atom Count:15
Complexity:243

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)C2=CC=C(O2)C=O

Technology Process of 5-Benzoyl-2-furancarboxaldehyde

There total 5 articles about 5-Benzoyl-2-furancarboxaldehyde 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: 91.0%

: 1002759-81-0
S-2-(tert-butylcarbamoyl)phenyl benzothioate

: 27329-70-0
5-formylfurane-2-boronic acid

: 13529-18-5
5-benzoyl-furan-2-carbaldehyde

Guidance literature:: With air; Cu(I)-3-methylsalicylate; In N,N-dimethyl-formamide; at 50 ℃;
DOI:10.1021/ja074931n

Reference yield: 61.0%

: 2689-65-8
5-iodofuran-2-carbaldehyde

: 98-88-4
benzoyl chloride

: 13529-18-5
5-benzoyl-furan-2-carbaldehyde

Guidance literature:: 5-iodofuran-2-carbaldehyde; With lithium dineopentylcuprate; In tetrahydrofuran; methanol; diethyl ether; at -78 ℃; for 0.25h;

benzoyl chloride; In tetrahydrofuran; methanol; diethyl ether; at 20 ℃; Further stages.;
DOI:10.1039/b604259g

Reference yield:

: 98-01-1
furfural

: 13529-18-5
5-benzoyl-furan-2-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / benzene / 12 h / Heating

In benzene;
DOI:10.1016/S0040-4020(01)91401-2