|
|
| | 2-Amino-4-bromobenzoic acid Basic information |
| | 2-Amino-4-bromobenzoic acid Chemical Properties |
| Melting point | 230-234 °C | | Boiling point | 352.4±32.0 °C(Predicted) | | density | 1.793±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | pka | 4.71±0.10(Predicted) | | form | powder to crystal | | color | White to Orange to Green | | Water Solubility | Soluble in water (slightly). | | Major Application | peptide synthesis | | InChI | InChI=1S/C7H6BrNO2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,9H2,(H,10,11) | | InChIKey | BNNICQAVXPXQAH-UHFFFAOYSA-N | | SMILES | C(O)(=O)C1=CC=C(Br)C=C1N | | CAS DataBase Reference | 20776-50-5(CAS DataBase Reference) |
| Hazard Codes | Xn | | Risk Statements | 22 | | Safety Statements | 36/37 | | RIDADR | UN 2811 6.1/PG 3 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29224999 | | Storage Class | 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | | Hazard Classifications | Acute Tox. 3 Oral |
| | 2-Amino-4-bromobenzoic acid Usage And Synthesis |
| Chemical Properties | slight yellow to white powder | | Uses | 2-Amino-4-bromobenzoic acid, , is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. | | reaction suitability | reaction type: solution phase peptide synthesis | | Synthesis | 2) Under stirring conditions, 4-bromo-2-nitrobenzoic acid (1.80 g, 7.83 mmol) was dissolved in 0.88 N aqueous sodium hydroxide (10 mL), followed by the sequential addition of ferric (III) chloride (133 mg) and isopropanol (0.7 mL). Hydrazine hydrate (1.1 mL) was slowly added dropwise to the above mixture and the reaction system was warmed up to 75 °C with continuous stirring for 2 hours. After completion of the reaction, the mixture was filtered and the filtrate was concentrated to give the crude product. The crude product was washed with water to afford 4-bromo-2-aminobenzoic acid (1.73 g, 96% yield). The structure of the product was confirmed by 1H NMR (DMSO-d6): δ 6.62 (dd, J = 1.5, 8.5 Hz, 1H), 6.95 (d, J = 1.5 Hz, 1H), 7.56 (d, J = 8.5 Hz, 1H). | | References | [1] Patent: US2004/116422, 2004, A1. Location in patent: Page/Page column 31
[2] Organic Letters, 2011, vol. 13, # 19, p. 5220 - 5223
[3] Journal of Organic Chemistry, 1997, vol. 62, # 5, p. 1240 - 1256
[4] Patent: WO2006/51290, 2006, A2. Location in patent: Page/Page column 111; 144
[5] Collection of Czechoslovak Chemical Communications, 1935, vol. 7, p. 436,443 |
| | 2-Amino-4-bromobenzoic acid Preparation Products And Raw materials |
|