- 4-BROMO-3-METHOXYANILINE
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- $1.10 / 1g
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2025-11-18
- CAS:19056-40-7
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons Min
- 4-BROMO-3-METHOXYANILINE
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- $15.00 / 1KG
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2021-07-02
- CAS:19056-40-7
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| | 4-BROMO-3-METHOXYANILINE Basic information |
| | 4-BROMO-3-METHOXYANILINE Chemical Properties |
| Melting point | 96-100 °C(lit.) | | Boiling point | 272.1±20.0 °C(Predicted) | | density | 1.531±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | form | solid | | pka | 3.47±0.10(Predicted) | | color | Beige | | BRN | 2690835 | | InChI | InChI=1S/C7H8BrNO/c1-10-7-4-5(9)2-3-6(7)8/h2-4H,9H2,1H3 | | InChIKey | RUTNWXBHRAIQSP-UHFFFAOYSA-N | | SMILES | C1(N)=CC=C(Br)C(OC)=C1 | | CAS DataBase Reference | 19056-40-7(CAS DataBase Reference) |
| Hazard Codes | Xn,Xi | | Risk Statements | 22-43 | | Safety Statements | 36/37 | | RIDADR | UN2811 | | WGK Germany | 2 | | Hazard Note | Irritant | | HazardClass | 6.1 | | PackingGroup | III | | HS Code | 29222990 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral
Skin Sens. 1 |
| | 4-BROMO-3-METHOXYANILINE Usage And Synthesis |
| Chemical Properties | White to brown crystalline powder | | Uses | 4-Bromo-3-(methyloxy)aniline is a useful reagent for organic synthesis and other chemical processes. It is used in the preparation of 4-Anilino substituted α-carboline compounds as active Brk inhibitors (breast tumor kinase) which are interesting targets for cancer therapy. | | Synthesis | General procedure for the synthesis of 4-bromo-3-methoxyaniline from 2-bromo-5-nitroanisole: To a solution of 1-bromo-2-methoxy-4-nitrobenzene (23 g, 99.6 mmol) in tetrahydrofuran (THF, 200 mL) was added ammonium chloride (64 g, 1.2 mol) and zinc powder (78.1 g, 1.2 mol). The reaction mixture was heated to reflux overnight. After completion of the reaction, the mixture was cooled to room temperature, filtered through a bed of diatomite (Celite) and the filtrate was concentrated under reduced pressure. The concentrated residue was partitioned between water (200 mL) and ethyl acetate (200 mL). The organic layer was separated, washed with brine solution (100 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 4-bromo-3-methoxyaniline (17.4 g, 87% yield) as a yellow solid. The product was confirmed by nuclear magnetic resonance hydrogen spectroscopy (1H NMR, DMSO-d6, 400 MHz): δ 7.1 (d, 1H), 6.31 (s, 1H), 6.1 (d, 1H), 5.27 (bs, 2H), 3.72 (s, 3H) ppm. | | References | [1] Patent: US4882354, 1989, A
[2] Patent: WO2015/6100, 2015, A1. Location in patent: Page/Page column 194
[3] Chemical and Pharmaceutical Bulletin, 2014, vol. 62, # 10, p. 979 - 988
[4] Patent: WO2007/37187, 2007, A1. Location in patent: Page/Page column 127
[5] Tetrahedron Letters, 1995, vol. 36, # 42, p. 7583 - 7586 |
| | 4-BROMO-3-METHOXYANILINE Preparation Products And Raw materials |
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