ChemicalBook >> CAS DataBase List >>2-Bromoterephthalic acid

2-Bromoterephthalic acid

CAS No.
586-35-6
Chemical Name:
2-Bromoterephthalic acid
Synonyms
BROMOTEREPHTHALIC ACID;DK7274;2-BromoterephthaL;2-BroMoterephthalic;LABOTEST-BB LT00454996;2-BROMOTEREPHTHALIC ACID;2-Bromotetraphenylquinone;Bromoterephthalic Acid >2-Bromoterephthalicacid,97%;2-BroMoterephthalic acid 95%
CBNumber:
CB5323524
Molecular Formula:
C8H5BrO4
Molecular Weight:
245.03
MDL Number:
MFCD00002403
MOL File:
586-35-6.mol
MSDS File:
SDS
Last updated:2026-05-28 04:45:16

2-Bromoterephthalic acid Properties

Melting point 295-297 °C(lit.)
Boiling point 421.6±40.0 °C(Predicted)
Density 1.8281 (rough estimate)
refractive index 1.4490 (estimate)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
pka 2.44±0.10(Predicted)
color White to Light yellow
Water Solubility Soluble in water.
BRN 2616163
InChI InChI=1S/C8H5BrO4/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3H,(H,10,11)(H,12,13)
InChIKey QPBGNSFASPVGTP-UHFFFAOYSA-N
SMILES C1(C(O)=O)=CC=C(C(O)=O)C=C1Br
CAS DataBase Reference 586-35-6(CAS DataBase Reference)
FDA UNII 7D55SB5C2G
UNSPSC Code 12352106
NACRES NA.23

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301-H315-H319-H335
Precautionary statements  P261-P264-P270-P301+P310-P302+P352-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard Codes  T,C,Xi
Risk Statements  25-36/37/38
Safety Statements  26-36-45-37/39
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
Hazard Note  Corrosive
HazardClass  6.1
HS Code  29173919
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
0
2 0

2-Bromoterephthalic acid price More Price(67)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 115274 2-Bromoterephthalic acid 95% 586-35-6 5g $121 2026-04-30 Buy
Sigma-Aldrich 8.41467 2-Bromoterephthalic acid for synthesis 586-35-6 25g $507 2026-04-30 Buy
Sigma-Aldrich 115274 2-Bromoterephthalic acid 95% 586-35-6 25g $399 2026-04-30 Buy
Sigma-Aldrich 8.41467 2-Bromoterephthalic acid for synthesis 586-35-6 5G $108 2024-03-01 Buy
TCI Chemical B1321 Bromoterephthalic Acid >98.0%(GC) 586-35-6 5g $136 2026-04-30 Buy
Product number Packaging Price Buy
115274 5g $121 Buy
8.41467 25g $507 Buy
115274 25g $399 Buy
8.41467 5G $108 Buy
B1321 5g $136 Buy

2-Bromoterephthalic acid Chemical Properties,Uses,Production

Chemical Properties

white crystalline powder

Uses

2-Bromoterephthalic acid is used as a biochemical for proteomics research. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, dyes and agrochemicals.

Synthesis

2,5-Dimethylbromobenzene

553-94-6

2-Bromoterephthalic acid

586-35-6

Example 6: This example describes in detail the synthesis of 2-bromoterephthalic acid using 2-bromo-1,4-dimethylbenzene as starting material. In a stirred autoclave equipped with an internal cooling coil and a reflux condenser, 2-bromo-1,4-dimethylbenzene (541 mmol) was mixed with 2-bromo-1,4-dimethylbenzene (541 mmol) containing cobalt(II) acetate tetrahydrate (0.625 mmol), manganese(II) acetate tetrahydrate (0.625 mmol), zirconium(IV) acetate (0.15 mmol) and sodium bromide (0.525 mmol) in a 500 g of 97% acetic acid solution were mixed. The mixture was stirred at a constant rate using a gas dispersion stirrer to optimize gas mixing, followed by heating the mixture to 150 °C for 2 h and maintaining it for 2 h, and then ramping up to 180 °C for 4 h. The mixture was heated to 150 °C for 2 h and then ramped up to 180 °C for 4 h. During the heating of the reaction, air was continuously vented at a back pressure of 400 psig (2.76 MPa). Upon completion of the reaction, the pressure was slowly released and the reactor was cooled to 50°C. The reaction products were drained and the reactor was rinsed with 50 g of acetic acid in two passes to collect the residual products. The white solid product was collected by diafiltration, washed with water and dried under vacuum, resulting in 113 g (85% yield) of a white solid of 2-bromoterephthalic acid with 99% purity, the structure of which was confirmed by 1H NMR.

References

[1] Patent: WO2008/82501, 2008, A1. Location in patent: Page/Page column 16-17
[2] Journal of Medicinal Chemistry, 2012, vol. 55, # 7, p. 3553 - 3557
[3] Journal of Coordination Chemistry, 2012, vol. 65, # 18, p. 3205 - 3215
[4] CrystEngComm, 2016, vol. 18, # 36, p. 6914 - 6925
[5] Patent: WO2015/97276, 2015, A1. Location in patent: Page/Page column 46; 47

Global( 248)Suppliers
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View Lastest Price from 2-Bromoterephthalic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Bromoterephthalic acid pictures 2019-08-08 2-Bromoterephthalic acid
586-35-6
$1.00 1KG 98% 100KG Career Henan Chemical Co
LABOTEST-BB LT00454996 2-BROMOTEREPHTHALIC ACID 2-BroMoterephthalic acid, 95% 25GR 2-Bromo-1,4-benzenedicarboxylic acid 2-Bromoterephthalic acid,99% 2-Bromoterephthalic acid,95% 2-BroMoterephthalic acid 95% 2-Bromoterephthalicacid,97% 2-bromobenzene-1,4-dicarboxylic acid 2-Bromoterephthalic acid 98+% 2-BroMoterephthalic 2-BromoterephthaL 1,4-Benzenedicarboxylicacid, 2-bromo- 2-Bromoterephthalic acid, 97.5% 2-Bromoterephthalic acid, 97.5%, for synthesis Bromoterephthalic Acid > DK7274 2-Bromotetraphenylquinone BROMOTEREPHTHALIC ACID 586-35-6 586-53-6 C8H5O4Br BrC6H314CO2H2 C8 Carbonyl Compounds Carboxylic Acids Building Blocks Organic Building Blocks Carboxylic Acid Monomers Monomers Polymer Science Phthalic Acids, Esters and Derivatives Acids & Esters Bromine Compounds Derivatives of phthalic acid