Benzoyl chloride, 4-(2-chloro-2-oxoethoxy)-

Base Information

Chemical Name:Benzoyl chloride, 4-(2-chloro-2-oxoethoxy)-
CAS No.:51822-12-9
Molecular Formula:C9H6Cl2O3
Molecular Weight:233.051
Hs Code.:
DSSTox Substance ID:DTXSID30451329
Nikkaji Number:J1.205.579J
Wikidata:Q82271302
Mol file:51822-12-9.mol

Synonyms:51822-12-9;Benzoyl chloride, 4-(2-chloro-2-oxoethoxy)-;SCHEMBL4360696;DTXSID30451329;(4-Chlorocarbonylphenoxy)acetic acid chloride

Suppliers and Price of Benzoyl chloride, 4-(2-chloro-2-oxoethoxy)-

Supply Marketing:

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

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Chemical Property of Benzoyl chloride, 4-(2-chloro-2-oxoethoxy)-

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:231.9693994
Heavy Atom Count:14
Complexity:222

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)Cl)OCC(=O)Cl

Technology Process of Benzoyl chloride, 4-(2-chloro-2-oxoethoxy)-

There total 2 articles about Benzoyl chloride, 4-(2-chloro-2-oxoethoxy)- 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%

: 19360-67-9
4-carboxymethoxy-benzoic acid

: 51822-12-9
4-chloroformylphenoxyacetyl chloride

Guidance literature:: With thionyl chloride; for 6h; Heating;
DOI:10.1080/00397919908085888

Reference yield:

: 99-96-7
4-hydroxy-benzoic acid

: 51822-12-9
4-chloroformylphenoxyacetyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / K₂CO₃; KI; polyethylene glycol-600 / toluene / 1.5 h / 105 - 110 °C

2: 91 percent / SOCl₂ / 6 h / Heating

With polyethylene glycol-600; thionyl chloride; potassium carbonate; potassium iodide; In toluene; 1: Substitution / 2: Chlorination;
DOI:10.1080/00397919908085888

Reference yield: 98.0%

: 51822-12-9
4-chloroformylphenoxyacetyl chloride

: 62-53-3
aniline

: N-phenyl-4-phenylcarbamoylmethoxy-benzamide

Guidance literature:: With polyethylene glycol-400; sodium hydroxide; In dichloromethane; water; at 20 ℃; for 1h;
DOI:10.1080/00397919908085888