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5-Bromosalicylic acid
Cas No: 89-55-4
USD $ 3.0-3.0 / Kilogram 1 Kilogram 1-100 Metric Ton/Month Dayang Chem (Hangzhou) Co.,Ltd. Contact Supplier
High quality 5-Bromosalicylic Acid supplier in China
Cas No: 89-55-4
No Data 1 Metric Ton 30 Metric Ton/Month Simagchem Corporation Contact Supplier
5-bromo-2-hydroxybenzoate
Cas No: 89-55-4
No Data 10 Milligram Amadis Chemical Co., Ltd. Contact Supplier
5-Bromosalicylic acid (COOH=1)
Cas No: 89-55-4
No Data No Data No Data Chemwill Asia Co., Ltd. Contact Supplier
5-Bromosalicylic acid CAS: 89-55-4
Cas No: 89-55-4
USD $ 1.0-2.0 / Metric Ton 5 Metric Ton 1000 Metric Ton/Year Henan Sinotech Import&Export Corporation Contact Supplier
Factory price CAS 89-55-4 5-Bromosalicylic acid in stock
Cas No: 89-55-4
USD $ 2000.0-2000.0 / Gram 1 Gram 1000 Metric Ton/Day Henan Tianfu Chemical Co., Ltd. Contact Supplier
Manufacturer supply CAS 89-55-4 with best quality
Cas No: 89-55-4
USD $ 139.0-210.0 / Kilogram 1 Kilogram 1000 Kilogram/Day Zhuozhou Wenxi import and Export Co., Ltd Contact Supplier
BLOOM TECH Advanced API/Technology support 5-Bromo-2-hydroxybenzoic acid CAS 89-55-4
Cas No: 89-55-4
No Data 1 Gram 3 Metric Ton/Month Shaanxi BLOOM TECH Co.,Ltd Contact Supplier
5-Bromosalicylic acid CAS NO.89-55-4
Cas No: 89-55-4
No Data 10 Gram 100 Kilogram/Week Jilin Tely Imp.& Exp.Co., Ltd. Contact Supplier
5-Bromosalicylic acid manufacturer
Cas No: 89-55-4
No Data No Data No Data Shaanxi Mingqi Chemical Co., Ltd Contact Supplier

89-55-4 Usage

Chemical Properties

WHITE TO SLIGHTLY BEIGE POWDER
InChI:InChI=1/C7H5BrO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)/p-1

89-55-4 Well-known Company Product Price

Brand (Code)Product description CAS number Packaging Price Detail
Alfa Aesar (B20338)  5-Bromosalicylic acid, 98%    89-55-4 250g 875.0CNY Detail
Alfa Aesar (B20338)  5-Bromosalicylic acid, 98%    89-55-4 100g 414.0CNY Detail
Alfa Aesar (B20338)  5-Bromosalicylic acid, 98%    89-55-4 50g 383.0CNY Detail

89-55-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromosalicylic Acid

1.2 Other means of identification

Product number -
Other names 5-bromo-2-hydroxybenzoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89-55-4 SDS

89-55-4Synthetic route

salicylic acid
69-72-7

salicylic acid

5-bromosalicyclic 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%
5-bromosalicyclaldehyde
1761-61-1

5-bromosalicyclaldehyde

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With sodium chlorite; sodium methylate In dimethyl sulfoxide84%
5-bromo-2-iodo-benzoic acid
21740-00-1

5-bromo-2-iodo-benzoic acid

5-bromosalicyclic 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%
2-hydroxy-5-bromobenzaldehyde oxime
82486-43-9

2-hydroxy-5-bromobenzaldehyde oxime

A

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

B

5-bromosalicyclaldehyde
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

4-bromo-2-propionylphenylmethylphenylcarbamate

A

N-methyl-N-phenylpropanamide
5827-78-1

N-methyl-N-phenylpropanamide

B

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

C

5-bromo-2-hydroxypropiophenone
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
tetrachloromethane
56-23-5

tetrachloromethane

4-bromo-phenol
106-41-2

4-bromo-phenol

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

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

n-butyllithium

diethyl ether
60-29-7

diethyl ether

2,4-dibromophenol
615-58-7

2,4-dibromophenol

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
anschliessend Behandeln mit festem Kohlendioxid;
2,4-dibromophenol
615-58-7

2,4-dibromophenol

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With n-butyllithium; diethyl ether anschliessendes Behandeln mit CO2;
phenyl 5-bromo-2-hydroxybenzoate
10268-63-0

phenyl 5-bromo-2-hydroxybenzoate

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
bei der Verseifung;
5-bromo-2-hydroxy-benzoic acid methyl ester
4068-76-2

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

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With sodium hydroxide
5-Bromo-2-aminobenzoic acid
5794-88-7

5-Bromo-2-aminobenzoic acid

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

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

salicylic acid

A

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

B

3,5-dibromosalicylic acid
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;
diethyl ether
60-29-7

diethyl ether

propyllithium
2417-93-8

propyllithium

2,4,6-tribromophenol
118-79-6

2,4,6-tribromophenol

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
anschliessend Behandeln mit festem Kohlendioxid;
2-hydroxy-benzoic acid ethyl ester
118-61-6

2-hydroxy-benzoic acid ethyl ester

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

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

salicylic acid

A

3-bromosalicylic acid
3883-95-2

3-bromosalicylic acid

B

5-bromosalicyclic acid
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.
salicylic acid
69-72-7

salicylic acid

A

3-bromosalicylic acid
3883-95-2

3-bromosalicylic acid

B

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

C

3,5-dibromosalicylic acid
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;
6-bromo-2,3-dimethyl-4H-chromen-4-one
99851-89-5

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

diluted alkali

diluted alkali

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

6-bromo-3-ethyl-2-methyl-4H-chromen-4-one
100953-68-2

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

alkaline solution

alkaline solution

A

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

B

2-Pentanone
107-87-9

2-Pentanone

phosphorus pentabromide
7789-69-7

phosphorus pentabromide

salicylic acid
69-72-7

salicylic acid

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

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

sulfuric acid

bromine
7726-95-6

bromine

acetic acid
64-19-7

acetic acid

salicylic acid
69-72-7

salicylic acid

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

bromine
7726-95-6

bromine

salicylic acid
69-72-7

salicylic acid

CS2

CS2

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

water
7732-18-5

water

hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

salicylic acid
69-72-7

salicylic acid

A

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

B

3,5-dibromosalicylic acid
3147-55-5

3,5-dibromosalicylic acid

bromine
7726-95-6

bromine

salicylic acid
69-72-7

salicylic acid

A

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

B

3,5-dibromosalicylic acid
3147-55-5

3,5-dibromosalicylic acid

bromine
7726-95-6

bromine

iodine
7553-56-2

iodine

acetic acid
64-19-7

acetic acid

salicylic acid
69-72-7

salicylic acid

A

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

B

3,5-dibromosalicylic acid
3147-55-5

3,5-dibromosalicylic acid

4-bromo-phenol
106-41-2

4-bromo-phenol

carbon dioxide
124-38-9

carbon dioxide

5-bromosalicyclic acid
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

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

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

diazotized 5-amino-salicylic acid

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

Conditions
ConditionsYield
With hydrogen bromide; copper
dipotassium salicylate

dipotassium salicylate

A

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

B

3,5-dibromosalicylic acid
3147-55-5

3,5-dibromosalicylic acid

Conditions
ConditionsYield
With potassium hypobromite
methanol
67-56-1

methanol

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

5-bromo-2-hydroxy-benzoic acid methyl ester
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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

allyl bromide
106-95-6

allyl bromide

C13H13BrO3

C13H13BrO3

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

5-bromosalicyclic acid

phenylboronic acid
98-80-6

phenylboronic acid

4-hydroxybiphenyl-3-carboxylic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

4-methylphenylboronic acid
5720-05-8

4-methylphenylboronic acid

5-(4-tolyl)salicylic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

2,4-difluorophenylboronic acid
144025-03-6

2,4-difluorophenylboronic acid

2',4'-difluoro-4-hydroxybiphenyl-3-carboxylic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

4-methoxyphenylboronic acid
5720-07-0

4-methoxyphenylboronic acid

4-hydroxy-4'-methoxy-[1,1'-biphenyl]-3-carboxylic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

hexadecanyl bromide
112-82-3

hexadecanyl bromide

5-hexadecylsalicylic acid
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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

acetyl chloride
75-36-5

acetyl chloride

2-acetyloxy-5-bromobenzoic acid
1503-53-3

2-acetyloxy-5-bromobenzoic acid

Conditions
ConditionsYield
With pyridine In dichloromethane98%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

alpha-bromo-3,4-difluorotoluene
85118-01-0

alpha-bromo-3,4-difluorotoluene

3,4-difluorobenzyl 5-bromo-2-(3,4-difluorobenzyloxy)benzoate
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;
1-Bromodocosane
6938-66-5

1-Bromodocosane

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

5-docosylsalicylic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

4-Chlorophenylboronic acid
1679-18-1

4-Chlorophenylboronic acid

4'-chloro-4-hydroxy-[1,1'-biphenyl]-3-carboxylic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

4-fluoroboronic acid
1765-93-1

4-fluoroboronic acid

2-hydroxy-5-(4'-fluorophenyl)benzoic 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%
o-fluorobenzyl bromide
446-48-0

o-fluorobenzyl bromide

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

2-fluorobenzyl 5-bromo-2-(2-fluorobenzyloxy)benzoate
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℃;
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

methyl iodide
74-88-4

methyl iodide

methyl 5-bromo-2-methoxybenzoate
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;
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

benzyl bromide
100-39-0

benzyl bromide

phenylmethyl 5-bromo-2-[(phenylmethyl)oxy]benzoate
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
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

tri(p-tolyl)bismuth
5142-75-6

tri(p-tolyl)bismuth

tris-p-tolylbismuth bis(5-bromosalicyate)

tris-p-tolylbismuth bis(5-bromosalicyate)

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

formaldehyd

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

5,5'-dibromo-3,3'-dicarboxy-2,2'-dihydroxydiphenylmethane
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;
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

3,5-difluorophenylboronic acid
156545-07-2

3,5-difluorophenylboronic acid

3',5'-difluoro-4-hydroxy-[1,1’-biphenyl]-3-carboxylic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

5-bromo-2-chlorobenzoic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

acetic anhydride
108-24-7

acetic anhydride

2-acetyloxy-5-bromobenzoic acid
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%
dichloromethane
75-09-2

dichloromethane

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

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

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%
tributyl borane
122-56-5

tributyl borane

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

5-n-butyl-2-hydroxybenzoic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

4-cyanobenzyl bromide
17201-43-3

4-cyanobenzyl bromide

4-cyanobenzyl 5-bromo-2-(4-cyanobenzyloxy)benzoate
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;
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

(meta-(trifluoromethyl)phenyl)boronic acid
1423-26-3

(meta-(trifluoromethyl)phenyl)boronic acid

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

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

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

5-bromosalicyclic acid

sulfamethizole
144-82-1

sulfamethizole

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

(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

terbium

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

terbium(III)(5-bromosalicylate)3

terbium(III)(5-bromosalicylate)3

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

gadolinium

5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

gadolinium(III)(5-bromosalicylate)3

gadolinium(III)(5-bromosalicylate)3

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

5-bromosalicyclic acid

2-acetyloxy-5-bromobenzoic 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%
5-bromosalicyclic acid
89-55-4

5-bromosalicyclic acid

ethyl 2-amino-4-(trifluoromethyl)-5-thiazole-carboxylate
344-72-9

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

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

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

Conditions
ConditionsYield
88.7%

89-55-4Downstream Products

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