ChemicalBook > CAS DataBase List > 2,6-DIBROMOBENZOIC ACID

2,6-DIBROMOBENZOIC ACID

Product Name
2,6-DIBROMOBENZOIC ACID
CAS No.
601-84-3
Chemical Name
2,6-DIBROMOBENZOIC ACID
Synonyms
2,6-DIBROMOBENZOIC ACID;Benzoic acid, 2,6-dibromo-;2,6-Dibromine Benzoic Acids;2,6-Dibromobenzoic Acid,>98%
CBNumber
CB2176602
Molecular Formula
C7H4Br2O2
Formula Weight
279.91
MOL File
601-84-3.mol
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2,6-DIBROMOBENZOIC ACID Property

Melting point:
151-152℃
Boiling point:
333.4±32.0 °C(Predicted)
Density 
1.9661 (rough estimate)
refractive index 
1.4970 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
1.50±0.10(Predicted)
color 
White to Light yellow
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Safety

HS Code 
2916399090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

TCI Chemical
Product number
D5485
Product name
2,6-Dibromobenzoic Acid
Packaging
1G
Price
$76
Updated
2025/07/31
TCI Chemical
Product number
D5485
Product name
2,6-Dibromobenzoic Acid
Packaging
5G
Price
$304
Updated
2025/07/31
TRC
Product number
D424490
Product name
2,6-Dibromobenzoic Acid
Packaging
50mg
Price
$85
Updated
2021/12/16
TRC
Product number
D424490
Product name
2,6-Dibromobenzoic Acid
Packaging
100mg
Price
$140
Updated
2021/12/16
TRC
Product number
D424490
Product name
2,6-Dibromobenzoic Acid
Packaging
5g
Price
$1375
Updated
2021/12/16
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2,6-DIBROMOBENZOIC ACID Chemical Properties,Usage,Production

Chemical Properties

Class white powder

Uses

2,6-Dibromobenzoic Acid is a reactant used in the synthesis of a novel inhibitor of amyloid secretion.

Synthesis

124-38-9

108-36-1

601-84-3

The general procedure for the synthesis of 2,6-dibromobenzoic acid from carbon dioxide and m-dibromobenzene was carried out as follows: the synthesis was carried out with reference to the literature method (Varcoe, J.R. et al., Chem. Mater. 2007, 19, 2686-2693). The procedure was as follows: anhydrous tetrahydrofuran (THF, 400 mL) was added to a two-necked round-bottomed flask under argon protection and cooled to 0 °C in an ice-water bath. Subsequently, n-butyllithium (2.5 M hexane solution, 117 mL) was added, followed by the slow addition of diisopropylamine (45 mL) at 0 °C to produce lithium diisopropylammonium (LDA). The reaction mixture was stirred for 45 min and then transferred to a dry ice/acetone bath to cool to -78 °C. At this temperature, 1,3-dibromobenzene (50.0 g, 0.212 mol) was added dropwise for a controlled period of 5 minutes and stirring was continued for 1 hour. Next, dry ice was sealed in a glass container and connected to the reaction mixture via a syringe. After bubbling gaseous CO2 into the reaction mixture for 45 min, dry ice was added. The reaction mixture was allowed to slowly warm up to room temperature. Aqueous sodium hydroxide solution (0.5 M) and ethyl acetate (400 mL) were added until all solids were dissolved. The aqueous layer was washed with ethyl acetate and acidified with concentrated hydrochloric acid to pH ≈ 1. The precipitate was dissolved in fresh ethyl acetate, washed with brine, dried over MgSO4, filtered and the solvent was evaporated under vacuum at 40°C. The solvent was then dried over MgSO4 and filtered. The resulting oil was cooled to room temperature and allowed to crystallize. The solid was boiled in hexane (2 L) for 1 hour and then cooled to room temperature. The solid was collected, washed with hexane and dried under vacuum at 80 °C to give 2,6-dibromobenzoic acid (39.3 g, 66% yield) as an off-white powder.1H NMR (500 MHz, DMSO-d6) δ 7.70 (d, J = 8.1 Hz, 2H), 7.29 (t, J = 8.1 Hz, 1H). 13C NMR (125 MHz, DMSO-d6) δ 166.87, 138.67, 131.87, 131.65.

References

[1] European Journal of Organic Chemistry, 2003, # 23, p. 4625 - 4629
[2] Organic Letters, 2009, vol. 11, # 5, p. 1051 - 1054
[3] Angewandte Chemie - International Edition, 2016, vol. 55, # 15, p. 4818 - 4821
[4] Angew. Chem., 2016, vol. 128, # 15, p. 4898 - 4902,5
[5] Patent: WO2017/117678, 2017, A1. Location in patent: Page/Page column 29; 34; 35

2,6-DIBROMOBENZOIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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2,6-DIBROMOBENZOIC ACID Suppliers

Energy Chemical
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021-021-58432009 400-005-6266
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021-58436166
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sales8178@energy-chemical.com
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China
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Shanghai Harvest Chemical Industrial Co., Ltd.
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021-31038972,31038973 17321035817
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+86-21-51385350
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sales@harvest-chem.com
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Shanghai Hanhong Scientific Co.,Ltd.
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021-54306202 13764082696
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info@hanhongsci.com
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Nanjing Vital Chemical Co., Ltd.
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Please Send Email 18652950785
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025-87193546
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TOKYO CHEMICAL INDUSTRY CO., LTD.
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03-3668-0520
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Japan
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TCI Europe
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sales@tcieurope.eu
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Europe
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SynAsst Chemical.
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Shanghai Yolne Chemical Co., Ltd.
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021-52212593
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934678158@qq.com
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Jalor-Chem co.,LTD
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0510-0510-86396359 13382276200
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View Lastest Price from 2,6-DIBROMOBENZOIC ACID manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
2,6-Dibromobenzoic acid 601-84-3
Price
US $0.00-0.00/KG
Min. Order
0.5KG
Purity
99%
Supply Ability
2000tons
Release date
2025-08-01
Career Henan Chemical Co
Product
2,6-DIBROMOBENZOIC ACID 601-84-3
Price
US $1.00/KG
Min. Order
1KG
Purity
98%-99.9%
Supply Ability
200kg
Release date
2020-01-12