Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Amides >  Naphthenic amines derivatives >  3-BROMO-4-METHOXYANILINE

3-BROMO-4-METHOXYANILINE

Basic information Safety Supplier Related

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
More
Less

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
More
Less

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
More
Less

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

3-BROMO-4-METHOXYANILINESupplier

GUANGZHOU AANPHARM TECHNOLOGY CO.,LTD Gold
Tel
020-86211473 13925088720
Email
linda@aanpharm.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
ShangHai DEMO Chemical Co.,Ltd
Tel
400-021-7337 2355568890
Email
sales@demochem.com
Beijing HwrkChemical Technology Co., Ltd
Tel
18515581800 18501085097
Email
sales.bj@hwrkchemical.com