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2840-02-0

2840-02-0 Structure

2840-02-0 Structure
IdentificationMore
[Name]

5-AMINO-2-BROMOBENZOIC ACID
[CAS]

2840-02-0
[Synonyms]

5-AMINO-2-BROMOBENZOIC
4-Bromo-3-carboxyaniline
5-AMINO-2-BROMOBENZOIC ACID
2-Bromo-5-aminobenzoic acid
Benzoic acid, 5-amino-2-bromo-
5-Amino-2-bromobenzoic acid 94%
5-AMINO-2-BROMOBENZOIC ACID USP/EP/BP
[Molecular Formula]

C7H6BrNO2
[MDL Number]

MFCD07368968
[Molecular Weight]

216.03
[MOL File]

2840-02-0.mol
Chemical PropertiesBack Directory
[Melting point ]

171-179 °C
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

Brown
[Water Solubility ]

Slightly soluble in water.
[InChI]

InChI=1S/C7H6BrNO2/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3H,9H2,(H,10,11)
[InChIKey]

FEXDUVBQBNYSQV-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC(N)=CC=C1Br
[CAS DataBase Reference]

2840-02-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
[RIDADR ]

UN 2811 6.1/PG 3
[WGK Germany ]

3
[Hazard Note ]

Harmful
[HazardClass ]

6.1
[HS Code ]

2922498590
Hazard InformationBack Directory
[Chemical Properties]

White crystalline solid
[Uses]

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs and is also used in medicine.
[reaction suitability]

reaction type: solution phase peptide synthesis
[Synthesis]

3-Aminobenzoic acid

99-05-8

5-AMINO-2-BROMOBENZOIC ACID

2840-02-0

General procedure for the synthesis of 5-amino-2-bromobenzoic acid from 3-aminobenzoic acid: 3-aminobenzoic acid (3.00 g, 21.9 mmol) was dissolved in N,N-dimethylformamide (18.0 mL) and cooled to below 5 °C. In another vessel, a solution was prepared by mixing N,N-dimethylformamide (9.00 mL) with N-bromosuccinimide (4.09 g, 23.0 mmol). This solution was slowly added to the cooled 3-aminobenzoic acid solution, keeping the reaction temperature at 5 °C or lower. The reaction mixture was stirred at 5 °C for 1 h. After the reaction mixture was stirred for 1 h, water (60.0 mL) was added and the stirring was continued for 12 h at 5 °C. Upon completion of the reaction, the solid product was collected by filtration, and the filtrate was washed with water (5.00 mL) and dried to give 5-amino-2-bromobenzoic acid (3.68 g, 78% yield). The structure of the product was confirmed by 1H-NMR (400 MHz, DMSO-D6): δ 5.49 (s, 2H), 6.59 (dd, J = 8.5,2.9Hz, 1H), 6.93 (d, J = 2.9Hz, 1H), 7.25 (d, J = 8.5Hz, 1H), 13.04 (s, 1H).

[Purification Methods]

Crystallise the acid from H2O or *C6H6 (m 128o). The acetyl derivative crystallises from H2O (as monohydrate) or absolute EtOH with m 196-197o (anhydrous). [Koopal Rec Trav Chim, Pays Bas 34 148 1915, Bamberger Chem Ber 57 2090 1924, Beilstein 14 H 413, 14 II 245.]
[References]

[1] Patent: US2013/310576, 2013, A1. Location in patent: Paragraph 0151
Spectrum DetailBack Directory
[Spectrum Detail]

5-AMINO-2-BROMOBENZOIC ACID(2840-02-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

2840-02-0(sigmaaldrich)
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