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89-55-4

Basic Information
CAS No.: 89-55-4
Name: Benzoic acid,5-bromo-2-hydroxy-
Molecular Structure:
Molecular Structure of 89-55-4 (Benzoic acid,5-bromo-2-hydroxy-)
Formula: C7H5BrO3
Molecular Weight: 217.03
Synonyms: Salicylicacid, 5-bromo- (6CI,8CI);2-Hydroxy-5-bromobenzoic acid;5-Bromo-2-hydroxybenzoic acid;NSC 3981;NSC 52393;
EINECS: 201-917-0
Density: 1.861 g/cm3
Melting Point: 162-166 °C
Boiling Point: 338.1 °C at 760 mmHg
Flash Point: 158.3 °C
Solubility: Soluble in water
Appearance: white to slightly beige powder
Hazard Symbols: IrritantXi
Risk Codes: 36/37/38
Safety: 37/39-26-36
Transport Information:
PSA: 57.53000
LogP: 1.85290
Synthetic route
69-72-7

salicylic acid

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With tetrapropylammonium nonabromide In dichloromethane at 23℃; for 0.5h; Inert atmosphere;95%
With sodium vanadate; aluminum tri-bromide; tetrabutylammomium bromide; oxygen In 1,4-dioxane; water at 80℃; for 8h; Reagent/catalyst; Solvent; Temperature;93.1%
With 1-butyl-3-methylpyridinium tribromide at 20℃; for 1h;89%
1761-61-1

5-bromosalicyclaldehyde

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With sodium chlorite; sodium methylate In dimethyl sulfoxide84%
21740-00-1

5-bromo-2-iodo-benzoic acid

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With copper(I) oxide; 1-D-O-Methyl-chiro-inositol; sodium hydroxide In water at 100℃; for 6h;77%
82486-43-9

2-hydroxy-5-bromobenzaldehyde oxime

A

89-55-4

5-bromosalicyclic acid

B

1761-61-1

5-bromosalicyclaldehyde

Conditions
ConditionsYield
With calcium hypochlorite; montmorillonite K-10 In chloroform at 20℃; for 4h;A 2.5%
B 69%

4-bromo-2-propionylphenylmethylphenylcarbamate

A

5827-78-1

N-methyl-N-phenylpropanamide

B

89-55-4

5-bromosalicyclic acid

C

17764-93-1

5-bromo-2-hydroxypropiophenone

Conditions
ConditionsYield
With water; sodium hydride In tetrahydrofuran for 24h; Reflux;A 60%
B 43%
C n/a
56-23-5

tetrachloromethane

106-41-2

4-bromo-phenol

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With sodium hydroxide
109-72-8, 29786-93-4

n-butyllithium

60-29-7

diethyl ether

615-58-7

2,4-dibromophenol

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
anschliessend Behandeln mit festem Kohlendioxid;
615-58-7

2,4-dibromophenol

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With n-butyllithium; diethyl ether anschliessendes Behandeln mit CO2;
10268-63-0

phenyl 5-bromo-2-hydroxybenzoate

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
bei der Verseifung;
4068-76-2

5-bromo-2-hydroxy-benzoic acid methyl ester

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With sodium hydroxide
5794-88-7

5-Bromo-2-aminobenzoic acid

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With hydrogenchloride; potassium nitrite
69-72-7

salicylic acid

A

89-55-4

5-bromosalicyclic acid

B

3147-55-5

3,5-dibromosalicylic acid

Conditions
ConditionsYield
With bromine; iodine; acetic acid
With bromine In acetic acid
With N-Bromosuccinimide; 1-n-butyl-3-methylimidazolim bromide for 0.0333333h; Ionic liquid;
With sulfuric acid; bromine at 20℃; for 1h; Reagent/catalyst; Temperature;A 94.5 %Chromat.
B 5 %Chromat.
Stage #1: salicylic acid In acetonitrile at 20℃; for 0.0833333h;
Stage #2: With N-Bromosuccinimide In acetonitrile at 20℃; for 16h; Solvent;
60-29-7

diethyl ether

2417-93-8

propyllithium

118-79-6

2,4,6-tribromophenol

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
anschliessend Behandeln mit festem Kohlendioxid;
118-61-6

2-hydroxy-benzoic acid ethyl ester

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With chloroform; bromine Behandeln mit alkoh. Kali;
69-72-7

salicylic acid

A

3883-95-2

3-bromosalicylic acid

B

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With tetrafluoroboric acid diethyl ether; N-Bromosuccinimide In acetonitrile for 5h; Ambient temperature; Yield given. Yields of byproduct given;
With sulfuric acid; bromine; acetic acid at 30℃; for 2h; Temperature;A 6.2 %Chromat.
B 87.6 %Chromat.
69-72-7

salicylic acid

A

3883-95-2

3-bromosalicylic acid

B

89-55-4

5-bromosalicyclic acid

C

3147-55-5

3,5-dibromosalicylic acid

Conditions
ConditionsYield
With N-Bromosuccinimide In acetonitrile for 5h; Ambient temperature;
With sulfuric acid; bromine; acetic acid at 30 - 60℃; for 0.5h;A 5.9 %Chromat.
B 88.1 %Chromat.
C 5.8 %Chromat.
With sulfuric acid; bromine at 3 - 25℃; for 1.5h; Reagent/catalyst; Temperature;A 1 %Chromat.
B 96 %Chromat.
C 3 %Chromat.
Stage #1: salicylic acid With sulfuric acid In dichloromethane at 20℃; for 0.0833333h;
Stage #2: With N-Bromosuccinimide In dichloromethane at 20℃; for 0.5h;
99851-89-5

6-bromo-2,3-dimethyl-4H-chromen-4-one

diluted alkali

diluted alkali

89-55-4

5-bromosalicyclic acid

100953-68-2

6-bromo-3-ethyl-2-methyl-4H-chromen-4-one

alkaline solution

alkaline solution

A

89-55-4

5-bromosalicyclic acid

B

107-87-9

2-Pentanone

7789-69-7

phosphorus pentabromide

69-72-7

salicylic acid

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
Behandeln des Produktes mit Wasser;
7664-93-9

sulfuric acid

7726-95-6

bromine

64-19-7

acetic acid

69-72-7

salicylic acid

89-55-4

5-bromosalicyclic acid

7726-95-6

bromine

69-72-7

salicylic acid

CS2

CS2

89-55-4

5-bromosalicyclic acid

10035-10-6, 12258-64-9

hydrogen bromide

7722-84-1

dihydrogen peroxide

69-72-7

salicylic acid

A

89-55-4

5-bromosalicyclic acid

B

3147-55-5

3,5-dibromosalicylic acid

7726-95-6

bromine

69-72-7

salicylic acid

A

89-55-4

5-bromosalicyclic acid

B

3147-55-5

3,5-dibromosalicylic acid

7726-95-6

bromine

7553-56-2

iodine

64-19-7

acetic acid

69-72-7

salicylic acid

A

89-55-4

5-bromosalicyclic acid

B

3147-55-5

3,5-dibromosalicylic acid

106-41-2

4-bromo-phenol

124-38-9

carbon dioxide

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With potassium carbonate at 140℃; under 29420.3 Torr;
aqueous 5-bromo-2-hydroxy-3-sulfo-benzoic acid

aqueous 5-bromo-2-hydroxy-3-sulfo-benzoic acid

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With overheated steam
diazotized 5-amino-salicylic acid

diazotized 5-amino-salicylic acid

89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With hydrogen bromide; copper
dipotassium salicylate

dipotassium salicylate

A

89-55-4

5-bromosalicyclic acid

B

3147-55-5

3,5-dibromosalicylic acid

Conditions
ConditionsYield
With potassium hypobromite
67-56-1

methanol

89-55-4

5-bromosalicyclic acid

4068-76-2

5-bromo-2-hydroxy-benzoic acid methyl ester

Conditions
ConditionsYield
With sulfuric acid Heating;100%
Stage #1: 5-bromosalicyclic acid With thionyl chloride In dichloromethane; N,N-dimethyl-formamide at 50℃; for 2h;
Stage #2: methanol for 0.5h; Solvent; Temperature;
100%
With sulfuric acid for 5h; Heating;95%
89-55-4

5-bromosalicyclic acid

106-95-6

allyl bromide

C13H13BrO3

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 80℃; for 17h;100%
89-55-4

5-bromosalicyclic acid

98-80-6

phenylboronic acid

323-87-5

4-hydroxybiphenyl-3-carboxylic acid

Conditions
ConditionsYield
With palladium diacetate; sodium carbonate In water at 20℃; for 2h;99%
With [Pd(N-(3-chloro-2-quinoxalinyl)-N'-(2,6-diisopropylphenyl)imidazolium)(PPh3)Cl2]; potassium carbonate In water at 70℃; for 3h; Catalytic behavior; Suzuki-Miyaura Coupling;98%
With potassium carbonate In water at 60℃; for 3h; Suzuki-Miyaura Coupling;96%
89-55-4

5-bromosalicyclic acid

5720-05-8

4-methylphenylboronic acid

43029-70-5

5-(4-tolyl)salicylic acid

Conditions
ConditionsYield
With 2C2H5NO2*Pd(2+)*2Cl(1-); potassium carbonate In water at 20℃; for 6h; Suzuki-Miyaura Coupling; Green chemistry;99%
With potassium carbonate In water at 20℃; for 4h; Suzuki-Miyaura Coupling; Green chemistry;95%
With potassium phosphate; 2-(dicyclohexylphosphino)biphenyl based D-gluconamide; palladium diacetate In water at 80℃; for 16h;87%
89-55-4

5-bromosalicyclic acid

144025-03-6

2,4-difluorophenylboronic acid

22494-42-4

2',4'-difluoro-4-hydroxybiphenyl-3-carboxylic acid

Conditions
ConditionsYield
With 2-[5-(4-methylphenyl)isoxazol-3-yl]-5-(5-phenylisoxazol-3-yl)-1,3,4-oxadiazole·2PdCl2; potassium carbonate In water; N,N-dimethyl-formamide at 100℃; for 0.0166667h; Suzuki Coupling;99%
With potassium carbonate; palladium dichloride In water; N,N-dimethyl-formamide at 75℃; Temperature; Solvent; Reagent/catalyst; Sonication; Cooling;98.37%
With C11H8Cl4N2O3Pd; potassium carbonate In methanol; water; N,N-dimethyl-formamide at 100℃; for 0.0833333h; Suzuki Coupling;97%
89-55-4

5-bromosalicyclic acid

5720-07-0

4-methoxyphenylboronic acid

25205-16-7

4-hydroxy-4'-methoxy-[1,1'-biphenyl]-3-carboxylic acid

Conditions
ConditionsYield
With 2C2H5NO2*Pd(2+)*2Cl(1-); sodium hydrogencarbonate In water at 20℃; for 6h; Suzuki-Miyaura Coupling; Green chemistry;99%
With [Pd(N-(3-chloro-2-quinoxalinyl)-N'-(2,6-diisopropylphenyl)imidazolium)(PPh3)Cl2]; potassium carbonate In water at 70℃; for 3h; Catalytic behavior; Suzuki-Miyaura Coupling;98%
With potassium carbonate In water at 20℃; for 4h; Suzuki-Miyaura Coupling; Green chemistry;96%
89-55-4

5-bromosalicyclic acid

112-82-3

hexadecanyl bromide

28294-58-8

5-hexadecylsalicylic acid

Conditions
ConditionsYield
Stage #1: hexadecanyl bromide With lithium In diethyl ether at -10℃; for 2h; Inert atmosphere;
Stage #2: With copper(l) iodide In diethyl ether at 0℃; for 1h; Inert atmosphere;
Stage #3: 5-bromosalicyclic acid In diethyl ether at 60℃; for 4h; Inert atmosphere;
98.1%
89-55-4

5-bromosalicyclic acid

75-36-5

acetyl chloride

1503-53-3

2-acetyloxy-5-bromobenzoic acid

Conditions
ConditionsYield
With pyridine In dichloromethane98%
89-55-4

5-bromosalicyclic acid

85118-01-0

alpha-bromo-3,4-difluorotoluene

1285517-06-7

3,4-difluorobenzyl 5-bromo-2-(3,4-difluorobenzyloxy)benzoate

Conditions
ConditionsYield
With potassium carbonate In acetone at 55℃; for 16h; Inert atmosphere;98%
With potassium carbonate In acetone at 20℃; for 15.5h; Product distribution / selectivity; Reflux;
6938-66-5

1-Bromodocosane

89-55-4

5-bromosalicyclic acid

5-docosylsalicylic acid

Conditions
ConditionsYield
Stage #1: 1-Bromodocosane With lithium In diethyl ether at -10℃; for 2h; Inert atmosphere;
Stage #2: With copper(l) iodide In diethyl ether at 10℃; for 1h; Inert atmosphere;
Stage #3: 5-bromosalicyclic acid In diethyl ether at 60℃; for 12h; Inert atmosphere;
97.9%
89-55-4

5-bromosalicyclic acid

1679-18-1

4-Chlorophenylboronic acid

4'-chloro-4-hydroxy-[1,1'-biphenyl]-3-carboxylic acid

Conditions
ConditionsYield
With [Pd(N-(3-chloro-2-quinoxalinyl)-N'-(2,6-diisopropylphenyl)imidazolium)(PPh3)Cl2]; potassium carbonate In water at 70℃; for 3h; Catalytic behavior; Suzuki-Miyaura Coupling;97%
89-55-4

5-bromosalicyclic acid

1765-93-1

4-fluoroboronic acid

22510-33-4

2-hydroxy-5-(4'-fluorophenyl)benzoic acid

Conditions
ConditionsYield
With sodium carbonate; palladium dichloride In water at 20℃; for 3h;96%
With potassium carbonate In water at 20℃; for 4h; Suzuki-Miyaura Coupling; Green chemistry;95%
With 2C2H5NO2*Pd(2+)*2Cl(1-); potassium carbonate In water at 20℃; for 6h; Suzuki-Miyaura Coupling; Green chemistry;91%
446-48-0

o-fluorobenzyl bromide

89-55-4

5-bromosalicyclic acid

1285517-00-1

2-fluorobenzyl 5-bromo-2-(2-fluorobenzyloxy)benzoate

Conditions
ConditionsYield
With potassium carbonate In acetone at 55℃; for 16h; Inert atmosphere;96%
With potassium carbonate In acetone at 70℃;
89-55-4

5-bromosalicyclic acid

74-88-4

methyl iodide

7120-41-4

methyl 5-bromo-2-methoxybenzoate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 6h;95%
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 14h; Inert atmosphere; Schlenk technique; Glovebox;75%
With potassium carbonate In N,N-dimethyl-formamide at 22℃; for 18h;
89-55-4

5-bromosalicyclic acid

100-39-0

benzyl bromide

850350-09-3

phenylmethyl 5-bromo-2-[(phenylmethyl)oxy]benzoate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h;95%
With potassium carbonate In acetone at 55℃; for 16h; Inert atmosphere;88%
With potassium carbonate In acetone at 70℃; Product distribution / selectivity;
With caesium carbonate In acetone for 2h; Reflux;15 g
89-55-4

5-bromosalicyclic acid

5142-75-6

tri(p-tolyl)bismuth

tris-p-tolylbismuth bis(5-bromosalicyate)

Conditions
ConditionsYield
With dihydrogen peroxide In diethyl ether; water at 20℃;93.3%
50-00-0

formaldehyd

89-55-4

5-bromosalicyclic acid

35232-55-4

5,5'-dibromo-3,3'-dicarboxy-2,2'-dihydroxydiphenylmethane

Conditions
ConditionsYield
In methanol 1.) 0 deg C, 2 h, 2.) RT, 14 h;93%
With sulfuric acid 1.) methanol, 1 h, 2.) methanol, water, 0 deg C, 4 h; Yield given. Multistep reaction;
89-55-4

5-bromosalicyclic acid

156545-07-2

3,5-difluorophenylboronic acid

3',5'-difluoro-4-hydroxy-[1,1’-biphenyl]-3-carboxylic acid

Conditions
ConditionsYield
With 2C2H5NO2*Pd(2+)*2Cl(1-); potassium carbonate In water at 20℃; for 6h; Suzuki-Miyaura Coupling; Green chemistry;93%
With potassium carbonate In water at 20℃; for 4h; Suzuki-Miyaura Coupling; Green chemistry;91%
89-55-4

5-bromosalicyclic acid

21739-92-4

5-bromo-2-chlorobenzoic acid

Conditions
ConditionsYield
With tetrachloromethane; molybdenum hexacarbonyl In dimethyl sulfoxide at 150℃; for 6h; Reagent/catalyst; Solvent; Autoclave;92.1%
89-55-4

5-bromosalicyclic acid

108-24-7

acetic anhydride

1503-53-3

2-acetyloxy-5-bromobenzoic acid

Conditions
ConditionsYield
With sulfuric acid In water at 20℃; for 0.666667h;92%
With sulfuric acid88%
With sulfuric acid88%
75-09-2

dichloromethane

89-55-4

5-bromosalicyclic acid

6-bromo-benzo[1,3]dioxin-4-one

Conditions
ConditionsYield
With potassium phosphate tribasic trihydrate In N,N-dimethyl-formamide at 100℃; under 760.051 Torr; for 6h; Green chemistry;92%
122-56-5

tributyl borane

89-55-4

5-bromosalicyclic acid

28488-45-1

5-n-butyl-2-hydroxybenzoic acid

Conditions
ConditionsYield
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate In tetrahydrofuran Suzuki coupling; Inert atmosphere; Reflux; chemoselective reaction;91%
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate In tetrahydrofuran Suzuki-Miyaura cross-coupling; Inert atmosphere; Reflux;91%
89-55-4

5-bromosalicyclic acid

17201-43-3

4-cyanobenzyl bromide

1285516-09-7

4-cyanobenzyl 5-bromo-2-(4-cyanobenzyloxy)benzoate

Conditions
ConditionsYield
With potassium carbonate In acetone at 55℃; for 16h; Inert atmosphere;91%
With potassium carbonate In acetone at 55℃; for 18h;
89-55-4

5-bromosalicyclic acid

1423-26-3

(meta-(trifluoromethyl)phenyl)boronic acid

4-Hydroxy-3'-trifluoromethyl-biphenyl-3-carboxylic acid

Conditions
ConditionsYield
With sodium carbonate; palladium at 80℃; for 5h;90%
89-55-4

5-bromosalicyclic acid

144-82-1

sulfamethizole

(E)-4-((5-bromo-2-hydroxybenzylidene)amino)-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide

Conditions
ConditionsYield
With toluene-4-sulfonic acid In ethanol at 78℃; for 6h;90%

terbium

89-55-4

5-bromosalicyclic acid

terbium(III)(5-bromosalicylate)3

Conditions
ConditionsYield
In acetonitrile at 30℃; Inert atmosphere; Sealed tube; Electrochemical reaction; Sonication;90%

gadolinium

89-55-4

5-bromosalicyclic acid

gadolinium(III)(5-bromosalicylate)3

Conditions
ConditionsYield
In acetonitrile at 30℃; Inert atmosphere; Sealed tube; Electrochemical reaction; Sonication;90%
89-55-4

5-bromosalicyclic acid

1503-53-3

2-acetyloxy-5-bromobenzoic acid

Conditions
ConditionsYield
With sodium chloride; sulfuric acid; acetic anhydride In water; ethyl acetate89%
With sodium chloride; sulfuric acid; acetic anhydride In water; ethyl acetate88%
89-55-4

5-bromosalicyclic acid

344-72-9

ethyl 2-amino-4-(trifluoromethyl)-5-thiazole-carboxylate

2-(5-bromo-2-hydroxybenzoyl)amino-4-(trifluoromethyl)thiazol-5-carboxylic acid ethylester

Conditions
ConditionsYield
88.7%
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  • 5-Bromosalicylic acid       CAS: 89-55-4

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    5-Bromosalicylic acid CAS: 89-55-4

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    CAS: 89-55-4 MF: C7H5BrO3 MW: 217.02 EINECS: 201-917-0 Mol File: 89-

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  • Casno:

    89-55-4

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    89-55-4

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    89-55-4

    5-Bromosalicylic acid

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    89-55-4

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    89-55-4

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    89-55-4

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    89-55-4

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    89-55-4

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    89-55-4

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    FOB Price:  USD $ 0.0-0.0/

    instock with good quality and wholesale price Storage:Keep in a cool & dry place Package:Packing material and QTY as your request Application:Pharma;Industry;other application Transportation:Express or as your request Port:Any port of China

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  •  Wuhan MoonZY Biological Technology Co.,Ltd

     China (Mainland)  |  Contact Details

    Business Type:Lab/Research institutions

    Tel:13545198479

    Address:203,Building 3, International Enterprise Center, No. 1 Guanshan 2nd Road, East Lake New Technology Development Zone,

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Chemistry

5-Bromosalicylic acid(89-55-4) is the chemical compound with the formula C7H5BrO3.Its molar weight is 217.02g/mol.
5-Bromosalicylic acid(89-55-4) is also named 2-Hydroxy-5-bromobenzoic acid;3-bromo-6-hydroxy-benzoicaci;5-bromo-2-hydroxy-benzoicaci;5-bromo-salicylicaci;Benzoic acid, 3-bromo-6-hydroxy-;Benzoic acid, 5-bromo-2-hydroxy-;Benzoicacid,5-bromo-2-hydroxy-;Salicylic acid, 5-bromo-.
Melting Point: 162-166 oC
Boiling Point: 338.1 oC at 760 mmHg
Flash Point: 158.3 oC
Water Solubility: Soluble
Index of Refraction: 1.654 
Molar Refractivity: 42.75 cm3 
Molar Volume: 116.5 cm3  
Surface Tension: 68.1 dyne/cm 
Density: 1.861 g/cm3 
Enthalpy of Vaporization: 61.36 kJ/mol 
Vapour Pressure: 3.93E-05 mmHg at 25 oC
The chemical structure of 5-Bromosalicylic acid(89-55-4) is
.

Uses

5-Bromosalicylic acid(89-55-4) is used as organic synthesis.

Toxicity Data With Reference

1.   

ivn-mus LD50:100 mg/kg

   CSLNX*    U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) NX#04478 .

Consensus Reports

Reported in EPA TSCA Inventory.

Safety Profile

Poison by intravenous route. When heated to decomposition it emits toxic fumes of Br.
Hazard Codes: Xi
Risk Statements: 36/37/38
36/37/38:  Irritating to eyes, respiratory system and skin  
Safety Statements: 37/39-26-36
37/39: Wear suitable gloves and eye/face protection 
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 
36: Wear suitable protective clothing 
RTECS: VO1850000.

Specification

5-Bromosalicylic acid(89-55-4)The extinguishing agents of 5-Bromosalicylic acid(89-55-4) is dry powder, carbon dioxide, water mist.