2,4-Dibromo-5-hydroxybenzoic acid

Base Information

• Chemical Name: 2,4-Dibromo-5-hydroxybenzoic acid
• CAS No.: 14348-39-1
• Molecular Formula: C7H4Br2O3
• Molecular Weight: 295.915
• Hs Code.: 2918290000
• DSSTox Substance ID: DTXSID40702738
• Nikkaji Number: J81.753H
• Wikidata: Q82634732
• Mol file: 14348-39-1.mol

Synonyms:2,4-Dibromo-5-hydroxybenzoic acid;14348-39-1;Benzoic acid, 2,4-dibromo-5-hydroxy-;2,4-Dibromo-5-hydroxybenzoicacid;DTXSID40702738;AKOS015998800;A884923

Chemical Property of 2,4-Dibromo-5-hydroxybenzoic acid

Chemical Property:

• PSA: 57.53000
• LogP: 2.61540
• Storage Temp.: Inert atmosphere,Room Temperature
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 295.85067
• Heavy Atom Count: 12
• Complexity: 186

Purity/Quality:

97% ^*data from raw suppliers

2,4-Dibromo-5-hydroxybenzoicacid 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C(=CC(=C1O)Br)Br)C(=O)O

Technology Process of 2,4-Dibromo-5-hydroxybenzoic acid

There total 8 articles about 2,4-Dibromo-5-hydroxybenzoic 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: 71.0%

3-Carboxyphenol (99-06-9) → 2,4-dibromo-5-hydroxybenzoic acid (14348-39-1)

Guidance literature:

With ammonium peroxodisulfate; sodium bromide; In water; at 20 ℃; for 6h; Irradiation;

Reference yield:

3-Carboxyphenol (99-06-9) → 2,4,6-tribromo-3-hydroxy-benzoic acid (14348-40-4) + 2,4-dibromo-5-hydroxybenzoic acid (14348-39-1)

Guidance literature:

With acetic acid; durch Bromierung;

Reference yield:

acetic acid (64-19-7,77671-22-8) + 3-Carboxyphenol (99-06-9) → 4-bromo-3-hydroxybenzoic acid (14348-38-0) + 2,4,6-tribromo-3-hydroxy-benzoic acid (14348-40-4) + 2,4-dibromo-5-hydroxybenzoic acid (14348-39-1)

Guidance literature:

upstream raw materials:

2,4-dibromo-5-hydroxybenzaldehyde

2,4-dibromo-5-methoxybenzoic acid

3-Carboxyphenol

acetic acid

Downstream raw materials:

2,4-dibromo-5-methoxybenzoic acid

4-hydroxy-3H-isobenzofuran-1-one

4-methoxyphthalide

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