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4-Bromophthalic acid

Basic Information

  • CAS No.: 6968-28-1

Physical properties

Product Description

Manufacturer supply good quality 4-Bromophthalic acid 6968-28-1 with stock

  • Molecular Formula: C8H5 Br O4
  • Molecular Weight: 245.029
  • Vapor Pressure: 1.54E-07mmHg at 25°C 
  • Melting Point: 162-164°C 
  • Refractive Index: 1.4490 (estimate) 
  • Boiling Point: 412.4oC at 760 mmHg 
  • PKA: 2.86±0.10(Predicted) 
  • Flash Point: 203.2oC 
  • PSA: 74.60000 
  • Density: 1.8281 (rough estimate) 
  • LogP: 1.84550 

4-Bromophthalic acid(Cas 6968-28-1) Usage

General Description

4-Bromophthalic acid, also known as 4-bromobenzoic acid-2-carboxylic acid or simply 4-bromo-2-carboxybenzoic acid, is a chemical compound that falls under the category of organobromides and benzene and substituted derivatives. Its molecular formula is C8H5BrO4 and it exhibits a molar mass of 249.03 g·mol?1. This acid appears as a solid and is mainly used in the field of organic synthesis. It is known to be a brominated derivative of phthalic acid. Since it's a chemical substance, appropriate safety precautions should be ensured while handling it to prevent exposure and possible associated hazards. It's recommended to always use personal protective equipment, and to work in a well-ventilated space or with approved equipment.

InChI:InChI=1/C8H5BrO4/c9-4-1-2-5(7(10)11)6(3-4)8(12)13/h1-3H,(H,10,11)(H,12,13)/p-2

6968-28-1 Relevant articles

Synthesis of 4-phenylethynylphthalic anhydride, a useful end-capping agent for polyimides

Yang, Mei-Jia,Shao, Tao,Men, Jian,Gao, Guo-Wei,Chen, Hua

, p. 379 - 380 (2012)

Hydrolysis and bromination of phthalic a...

CYCLIC PEPTIDE ANALOGS OF MELANOCORTIN AND AMANITIN AND METHODS OF MAKING SUCH

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Paragraph 0114-0115; 0122, (2021/01/29)

The invention described herein is based ...

Fluorescent Isoindole Crosslink (FlICk) Chemistry: A Rapid, User-friendly Stapling Reaction

Todorovic, Mihajlo,Schwab, Katerina D.,Zeisler, Jutta,Zhang, Chengcheng,Bénard, Francois,Perrin, David M.

supporting information, p. 14120 - 14124 (2019/07/31)

The stabilization of peptide secondary s...

Synthesis and biological evaluation of chemokine receptor ligands with 2-benzazepine scaffold

Thum, Simone,Kokornaczyk, Artur K.,Seki, Tomoaki,De Maria, Monica,Ortiz Zacarias, Natalia V.,de Vries, Henk,Weiss, Christina,Koch, Michael,Schepmann, Dirk,Kitamura, Masato,Tschammer, Nuska,Heitman, Laura H.,Junker, Anna,Wünsch, Bernhard

supporting information, p. 401 - 413 (2017/05/04)

Targeting CCR2 and CCR5 receptors is con...

Industrial preparation method of 5-bromophthalide

-

Paragraph 0012; 0013; 0014; 0015; 0016, (2017/09/01)

The invention relates to a preparation m...

6968-28-1 Process route

phthalic anhydride
85-44-9

phthalic anhydride

4-bromophthalic acid
6968-28-1

4-bromophthalic acid

Conditions
Conditions Yield
With bromine; sodium hydroxide; In water; for 72h; Reflux;
95%
phthalic anhydride; With sodium hydroxide; In water; at 40 - 95 ℃; for 1h;
With bromine; In water; at 40 - 95 ℃; Temperature; Reagent/catalyst;
70.9%
phthalic anhydride; With bromine; sodium hydroxide; In water; at 90 ℃; for 7h;
With hydrogenchloride; In water; pH=Ca. 1.5;
68%
phthalic anhydride; With sodium hydroxide; In water;
With bromine; In water; at 90 ℃; for 7h;
With hydrogenchloride; In water;
68%
With sodium hydroxide; bromine;
phthalic anhydride; With sodium hydroxide; In water;
With bromine; In water; at 20 - 90 ℃;
With hydrogenchloride; In water;
Multi-step reaction with 2 steps
1: sodium hydroxide; bromine / water / 7 h / 90 °C
2: hydrogenchloride / water
With hydrogenchloride; bromine; sodium hydroxide; In water;
2-bromonaphthalene
580-13-2

2-bromonaphthalene

4-bromophthalic acid
6968-28-1

4-bromophthalic acid

Conditions
Conditions Yield
With sodium hypochlorite; ruthenium(III) chloride trihydrate; sulfuric acid; tetrabutylammomium bromide; In water; 1,2-dichloro-ethane; at 23 ℃; for 0.333333h; pH=9; Green chemistry;
52%

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