ChemicalBook--->CAS DataBase List--->50419-88-0

50419-88-0

50419-88-0 Structure

50419-88-0 Structure
IdentificationBack Directory
[Name]

BUTTPARK 80\07-66
[CAS]

50419-88-0
[Synonyms]

BUTTPARK 80\07-66
4-Chloro-5-bromoanthranilic acid
2-AMINO-5-BROMO-4-CHLOROBENZOIC ACID
BENZOIC ACID, 2-AMINO-5-BROMO-4-CHLORO-
2-amino-5-bromo-4-chlorobenzene carboxylic acid
[Molecular Formula]

C7H5BrClNO2
[MDL Number]

MFCD06409111
[MOL File]

50419-88-0.mol
[Molecular Weight]

250.48
Chemical PropertiesBack Directory
[Boiling point ]

385.0±42.0 °C(Predicted)
[density ]

1.892
[storage temp. ]

2-8°C, protect from light
[pka]

4.32±0.10(Predicted)
[Appearance]

Off-white to light brown Solid
Spectrum DetailBack Directory
[Spectrum Detail]

BUTTPARK 80\07-66(50419-88-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-4-chlorobenzoic acid

89-77-0

BUTTPARK 80\07-66

50419-88-0

2-Amino-4-chlorobenzoic acid (I; 20.00 g, 116.6 mmol) and acetonitrile (300 mL) were added to a 500 mL single-necked round-bottomed flask with rapid stirring to form a beige-colored suspension. At room temperature, N-bromosuccinimide (NBS; 20.75 g, 116.6 mmol) was added slowly in batches. After addition, the reaction mixture was continued to be stirred for 1 hour. Subsequently, the reaction mixture was placed in a 45 °C water bath and the solvent was removed by rotary evaporation. Water was added to the residue, stirred and the filter cake was washed by filtration. Finally, the product was dried under vacuum at 60 °C to afford 2-amino-5-bromo-4-chlorobenzoic acid (II; 28.62 g, 98% yield).

[References]

[1] Patent: CN106986809, 2017, A. Location in patent: Paragraph 0024; 0025; 0026; 0027; 0028; 0029; 0030
[2] Patent: CN106966914, 2017, A. Location in patent: Paragraph 0019; 0020; 0028; 0029; 0036; 0037
[3] Patent: US2015/119405, 2015, A1. Location in patent: Paragraph 0407; 0408; 0409
[4] Patent: WO2005/54238, 2005, A1. Location in patent: Page/Page column 70
[5] Organic and Biomolecular Chemistry, 2014, vol. 12, # 27, p. 5031 - 5037
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