3,5-Bis(acetyloxy)benzoyl chloride

Base Information

Chemical Name:3,5-Bis(acetyloxy)benzoyl chloride
CAS No.:39192-49-9
Molecular Formula:C11H9ClO5
Molecular Weight:256.642
Hs Code.:
European Community (EC) Number:855-283-0
DSSTox Substance ID:DTXSID70463805
Nikkaji Number:J674.225D
Wikidata:Q82288850
Mol file:39192-49-9.mol

Synonyms:3,5-bis(acetyloxy)benzoyl chloride;39192-49-9;3,5-DIACETOXYBENZOYL CHLORIDE;Benzoyl chloride, 3,5-bis(acetyloxy)-;(3-acetyloxy-5-carbonochloridoylphenyl) acetate;3,5-diacetoxybenzoylchloride;SCHEMBL392901;3,5-Diacetoxy benzoyl chloride;DTXSID70463805;QFBUFKRWGXGPEH-UHFFFAOYSA-N

Suppliers and Price of 3,5-Bis(acetyloxy)benzoyl chloride

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 3,5-Bis(acetyloxy)benzoyl chloride

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:256.0138511
Heavy Atom Count:17
Complexity:304

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1=CC(=CC(=C1)C(=O)Cl)OC(=O)C

Technology Process of 3,5-Bis(acetyloxy)benzoyl chloride

There total 5 articles about 3,5-Bis(acetyloxy)benzoyl chloride 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: 98.2%

: 35354-29-1
3,5-diacetoxybenzoic acid

: 39192-49-9
3,5-diacetoxybenzoyl chloride

Guidance literature:: With thionyl chloride; In dichloromethane; Reflux;

Reference yield:

: 99-10-5
3,5-Dihydroxybenzoic acid

: 39192-49-9
3,5-diacetoxybenzoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 4 h / 20 °C

2: SOCl₂ / CH₂Cl₂ / 3 h / Heating

With pyridine; thionyl chloride; In dichloromethane;
DOI:10.1248/cpb.53.1402