ChemicalBook--->CAS DataBase List--->232275-51-3

232275-51-3

232275-51-3 Structure

232275-51-3 Structure
IdentificationBack Directory
[Name]

4-BROMO-2,6-DICHLOROBENZOIC ACID
[CAS]

232275-51-3
[Synonyms]

4-BROMO-2,6-DICHLOROBENZOIC ACID
Benzoic acid, 4-broMo-2,6-dichloro-
4-Bromo-2,6-dichlorobenzoic Acid >
[Molecular Formula]

C7H3BrCl2O2
[MDL Number]

MFCD11227148
[MOL File]

232275-51-3.mol
[Molecular Weight]

269.91
Chemical PropertiesBack Directory
[Melting point ]

165.0 to 169.0 °C
[Boiling point ]

336.7±42.0 °C(Predicted)
[density ]

1.900
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

1.40±0.25(Predicted)
[color ]

White to Orange to Green
[CAS DataBase Reference]

232275-51-3
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2916.39.7900
Spectrum DetailBack Directory
[Spectrum Detail]

4-Bromo-2,6-dichlorobenzoic acid(232275-51-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-amino-4-bromo-2,6-dichlorobenzoic acid

1415124-69-4

4-Bromo-2,6-dichlorobenzoic acid

232275-51-3

Step d: Synthesis of 4-bromo-2,6-dichlorobenzoic acid Aqueous sodium nitrite solution (3.64 g, 52 mmol, dissolved in 4 mL of water) was added dropwise to concentrated hydrochloric acid (15 mL) and cooled to -10°C to -5°C. 3-Amino-4-bromo-2,6-dichlorobenzoic acid (5 g, 17 mmol, product of step c) was added in batches to the above solution while controlling the reaction temperature to maintain it at about -5°C. The reaction mixture was stirred at this temperature for 2 hours. Subsequently, hypophosphorous acid (9 mL, 170 mmol) was added slowly and dropwise over 1 h at the same temperature. The reaction mixture was stirred at the same temperature for 3 hours and then transferred to a refrigerator and allowed to stand overnight. Precipitation generation was observed at this stage. The reaction mixture was slowly warmed up to room temperature and stirring was continued for 2 hours at room temperature. The reaction mixture was filtered and the resulting solid was washed with cold water and dried to afford 4-bromo-2,6-dichlorobenzoic acid as a pale yellow solid (2 g, 42% yield).1H NMR (400 MHz, MeOH-d4): δ 7.69 (s, 2H).

[References]

[1] Patent: WO2012/160464, 2012, A1. Location in patent: Page/Page column 62-63; 80
[2] Patent: US2014/155398, 2014, A1. Location in patent: Paragraph 0384; 0480
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