5-(Octyloxy)benzene-1,3-dicarbonyl dichloride

Base Information

Chemical Name:5-(Octyloxy)benzene-1,3-dicarbonyl dichloride
CAS No.:87322-89-2
Molecular Formula:C16H20Cl2O3
Molecular Weight:331.239
Hs Code.:
DSSTox Substance ID:DTXSID80573560
Nikkaji Number:J1.668.638G
Wikidata:Q82462307

Synonyms:87322-89-2;5-octyloxyisophthaloyldichloride;5-(OCTYLOXY)BENZENE-1,3-DICARBONYL DICHLORIDE;DTXSID80573560

Suppliers and Price of 5-(Octyloxy)benzene-1,3-dicarbonyl dichloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-(Octyloxy)benzene-1,3-dicarbonyl dichloride

Chemical Property:

XLogP3:6.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:10
Exact Mass:330.0789499
Heavy Atom Count:21
Complexity:312

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCOC1=CC(=CC(=C1)C(=O)Cl)C(=O)Cl

Technology Process of 5-(Octyloxy)benzene-1,3-dicarbonyl dichloride

There total 2 articles about 5-(Octyloxy)benzene-1,3-dicarbonyl dichloride 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: 79.7%

: 181627-67-8
5-(octyloxy)isophthalic acid

: 87322-89-2
5-octyloxy-1,3-benzenedicarbonyl chloride

Guidance literature:: With thionyl chloride; In DMF (N,N-dimethyl-formamide); at 50 - 75 ℃; for 3h; Heating / reflux;

Reference yield:

: 111-83-1
1-bromo-octane

: 39630-68-7
diethyl 5-hydroxyisophthalate

: 87322-89-2
5-octyloxy-1,3-benzenedicarbonyl chloride

Guidance literature:: 1-bromo-octane; diethyl 5-hydroxyisophthalate; With potassium carbonate; In acetone;

With water; Alkaline hydrolysis;

With oxalyl dichloride;
DOI:10.1016/j.tetlet.2006.03.044