3-BROMO-4-METHOXYANILINE
3-BROMO-4-METHOXYANILINE Basic information
- Product Name:
- 3-BROMO-4-METHOXYANILINE
- Synonyms:
-
- 3-BROMO-4-METHOXYANILINE
- 4-Amino-2-bromoanisole
- 4-Amino-2-bromoanisole, 3-Bromo-p-anisidine
- 3-Bromo-4-methoxyaniline >
- Benzenamine, 3-bromo-4-methoxy-
- 3-BROMO-4-METHOXYANILINE ISO 9001:2015 REACH
- 3-Bromo-4-methoxyanilin
- CAS:
- 19056-41-8
- MF:
- C7H8BrNO
- MW:
- 202.05
- Product Categories:
-
- Phenyls & Phenyl-Het
- Amines
- Phenyls & Phenyl-Het
- Mol File:
- 19056-41-8.mol
3-BROMO-4-METHOXYANILINE Chemical Properties
- Melting point:
- 62 °C
- Boiling point:
- 282.2±20.0 °C(Predicted)
- Density
- 1.531±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 4.13±0.10(Predicted)
- color
- White to Brown
- InChIKey
- NMUFTXMBONJQTC-UHFFFAOYSA-N
- CAS DataBase Reference
- 19056-41-8
Safety Information
- Hazard Codes
- Xi,N,T+
- Risk Statements
- 26/27/28-33-50
- Safety Statements
- 28-36/37-45-61
- RIDADR
- 2811
- HazardClass
- IRRITANT
- PackingGroup
- III
- HS Code
- 2921420090
3-BROMO-4-METHOXYANILINE Usage And Synthesis
Uses
3-Bromo-4-methoxyaniline is an intermediate used to prepare triazole analogs of combretastatin A-4 as cytotoxic agents and inhibitors of tubulin. It is also used in the synthesis of (1,2,4-oxadiazolyl)biphenylcarbonyltetrahydrospiro[furo]indolepiperidine (SB-224289) as selective 5-HT1B receptor inverse agonist.
Synthesis
5197-28-4
19056-41-8
General procedure for the synthesis of 3-bromo-4-methoxyaniline from 2-bromo-4-nitroanisole: 2-bromo-4-nitroanisole (0.1 g, 0.43 mmol) was suspended in unstabilized 57% hydriodic acid (1.3 mL), and the reaction was heated for 5 hr at 90 °C. After completion of the reaction, the reaction mixture was cooled, diluted with ethyl acetate (5 mL) and washed sequentially with saturated aqueous sodium thiosulfate and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated. The crude product was further purified by silica gel column chromatography to afford 3-bromo-4-methoxyaniline (0.07 g, 80% yield).
References
[1] ACS Catalysis, 2015, vol. 5, # 3, p. 1526 - 1529
[2] Patent: WO2011/98776, 2011, A1. Location in patent: Page/Page column 60
[3] Patent: US2013/53372, 2013, A1. Location in patent: Paragraph 0584; 0585
[4] Patent: US2007/123515, 2007, A1. Location in patent: Page/Page column 24
[5] Justus Liebigs Annalen der Chemie, 1883, vol. 217, p. 44
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3-BROMO-4-METHOXYANILINE(19056-41-8)Related Product Information
- EOSIN B
- 2-Bromo-4-nitroanisole
- EOSIN B
- 2-BROMO-5-METHOXYANILINE
- 5-Bromo-2-methoxyaniline, HCl
- 2-BROMO-4-METHOXYANILINE
- 2-bromo-5-aminoanisole(4-bromo-3-methoxyaniline),4-BROMO-3-METHOXYANILINE, 98+%,4-Bromo-3-methoxyaniline, 97+%,4-BROMO-3-METHOXYANILINE
- 4-BROMO-2-METHOXYANILINE[2-AMINO-5-BROMOANISOLE] ,4-BROMO-2-METHOXYANILINE
- 2-Bromo-5-methoxyaniline, HCl
- 5-BROMO-2-METHOXYANILINE
- 2-Bromoanisole
- 3-BROMO-4-(TRIFLUOROMETHOXY)ANILINE
- 1,3-DIBROMO-2-METHOXY-5-NITROBENZENE
- 2-BROMO-1-(4-FLUOROPHENOXY)-4-NITROBENZENE
- 3-Bromo-4-methoxyaniline hydrochloride
- 2-BROMO-3-METHOXYANILINE HYDROCHLORIDE
- 2-BROMO-5-METHOXYANILINE SULPHATE
- 2-BROMO-6-METHOXYANILINE