5-(Benzoyloxy)benzene-1,3-dicarboxylic acid

Base Information

Chemical Name:5-(Benzoyloxy)benzene-1,3-dicarboxylic acid
CAS No.:102059-70-1
Molecular Formula:C15H10 O6
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID70478454
Wikidata:Q82311848
Mol file:102059-70-1.mol

Synonyms:5-(Benzoyloxy)benzene-1,3-dicarboxylic acid;102059-70-1;5-benzoyloxybenzene-1,3-dicarboxylic acid;DTXSID70478454

Suppliers and Price of 5-(Benzoyloxy)benzene-1,3-dicarboxylic acid

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
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price

Total 1 raw suppliers

Chemical Property of 5-(Benzoyloxy)benzene-1,3-dicarboxylic acid

Chemical Property:

PSA：100.90000
LogP:2.30220
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:286.04773803
Heavy Atom Count:21
Complexity:390

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)OC2=CC(=CC(=C2)C(=O)O)C(=O)O

Technology Process of 5-(Benzoyloxy)benzene-1,3-dicarboxylic acid

There total 1 articles about 5-(Benzoyloxy)benzene-1,3-dicarboxylic 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:

Reference yield: 92.0%

: 618-83-7
5-Hydroxyisophthalic acid

: 98-88-4
benzoyl chloride

: 102059-70-1
5-(benzoyloxy)isophthalic acid

Guidance literature:: With sodium hydroxide; In diethyl ether; water; at 20 ℃; for 4h;
DOI:10.1002/1615-4169(20010330)343:3<303::AID-ADSC303>3.0.CO;2-G

Reference yield: 19.0%

: 102059-70-1
5-(benzoyloxy)isophthalic acid

: 101923-70-0
5-(benzoyloxy)isophthaloyl dichloride

Guidance literature:: With thionyl chloride; N,N-dimethyl-formamide; for 2h; Heating;
DOI:10.1002/1615-4169(20010330)343:3<303::AID-ADSC303>3.0.CO;2-G

Reference yield:

: 102059-70-1
5-(benzoyloxy)isophthalic acid

: 865365-50-0
N¹,N³-bis(6-butyramidopyridin-2-yl)-5-hydroxyisophthalamide

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂; DMF / 5 h / Heating

2: 3.2 g / triethylamine / tetrahydrofuran / 12 h / Heating

3: 61 percent / KOH / dioxane; H₂O / 48 h / 20 °C

With potassium hydroxide; thionyl chloride; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; water;
DOI:10.1002/ejoc.200500951