4-Chloro-2-hydroxybenzoyl chloride

Base Information

• Chemical Name: 4-Chloro-2-hydroxybenzoyl chloride
• CAS No.: 82944-13-6
• Molecular Formula: C7H4 Cl2 O2
• Molecular Weight: 191.014
• Hs Code.: 2918290000
• European Community (EC) Number: 893-340-1
• DSSTox Substance ID: DTXSID90513119
• Nikkaji Number: J1.217.466G
• Wikidata: Q82372732
• Mol file: 82944-13-6.mol

Synonyms:4-Chloro-2-hydroxybenzoyl chloride;82944-13-6;MFCD11169660;SCHEMBL4880939;DTXSID90513119;4-Chloro-2-hydroxybenzoylchloride;CCBOXJLPEZRSSA-UHFFFAOYSA-N;AKOS009216403;LS-11824;A915529

Chemical Property of 4-Chloro-2-hydroxybenzoyl chloride

Chemical Property:

• PSA: 37.30000
• LogP: 2.42460
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 189.9588348
• Heavy Atom Count: 11
• Complexity: 161

Purity/Quality:

99%, ^*data from raw suppliers

4-Chloro-2-hydroxybenzoyl chloride 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1Cl)O)C(=O)Cl

Technology Process of 4-Chloro-2-hydroxybenzoyl chloride

There total 1 articles about 4-Chloro-2-hydroxybenzoyl 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:

4-chlorosalicylic acid (5106-98-9) → 4-chloro-2-hydroxybenzoyl chloride (82944-13-6)

Guidance literature:

With thionyl chloride; N,N-dimethyl-formamide; In n-heptane; at 60 ℃;

DOI:10.1016/j.bmc.2004.07.062

Reference yield: 99.0%

4-chloro-2-hydroxybenzoyl chloride (82944-13-6) + (4-trifluoromethylsulfanyl-phenoxy)-acetic acid hydrazide → 4-chloro-2-hydroxy-benzoic acid N'-[(4-trifluoromethylsulfanyl-phenoxy)-acetyl]-hydrazide

Guidance literature:

With 4-vinylpyridine; In tetrahydrofuran; at 20 ℃;

DOI:10.1016/S0040-4039(99)01972-3

Reference yield: 97.0%

4-sec-butylaniline (30273-11-1,181288-08-4) + 4-chloro-2-hydroxybenzoyl chloride (82944-13-6) → N-(4-sec-butyl-phenyl)-4-chloro-2-hydroxy-benzamide

Guidance literature:

With 4-vinylpyridine; In tetrahydrofuran; at 20 ℃;

DOI:10.1016/S0040-4039(99)01972-3

upstream raw materials:

4-chlorosalicylic acid

Downstream raw materials:

N-benzyl-4-chloro-2-hydroxybenzamide

4-chloro-N-(4-chlorobenzyl)salicylamide

4-chloro-N-(4-methoxybenzyl)salicylamide

4-chloro-N-(3,4-dichlorobenzyl)salicylamide

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