3-bromo-2-methoxyaniline

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Company Name: Shaanxi Dideu Medichem Co. Ltd
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Products Intro: Product Name:3-bromo-2-methoxyaniline
CAS:116557-46-1
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Products Intro: Product Name:3-bromo-2-methoxyaniline
CAS:116557-46-1
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Products Intro: Product Name:2-amino-6-bromoanisole
CAS:116557-46-1
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CAS:116557-46-1
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Products Intro: Product Name:3-Bromo-2-methoxybenzenamine
CAS:116557-46-1
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG

3-bromo-2-methoxyaniline manufacturers

  • 3-bromo-2-methoxyaniline
  • 3-bromo-2-methoxyaniline pictures
  • $0.10 / 1KG
  • 2025-09-02
  • CAS:116557-46-1
  • Min. Order: 0.100000001490116KG
  • Purity: 98%
  • Supply Ability: 200TONS
3-bromo-2-methoxyaniline Basic information
Product Name:3-bromo-2-methoxyaniline
Synonyms:3-Bromo-2-methoxybenzenamine;2-Amino-6-bromoanisole, 3-Bromo-o-anisidine;2-amino-6-bromoanisole;BenzenaMine, 3-broMo-2-Methoxy-;3-Bromo-o-anisidine;3-bromo-2-methoxyphenylamine hydrochloride;3-Bromo-2-methoxy-phenylamine;3-BROMO-2-METHOXYANILINE
CAS:116557-46-1
MF:C7H8BrNO
MW:202.05
EINECS:229-486-4
Product Categories:
Mol File:116557-46-1.mol
3-bromo-2-methoxyaniline Structure
3-bromo-2-methoxyaniline Chemical Properties
Melting point 65℃
Boiling point 268℃
density 1.531
refractive index 1.5430 to 1.5470
Fp 116℃
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka3.46±0.10(Predicted)
form clear liquid
color Light yellow to Brown
InChIInChI=1S/C7H8BrNO/c1-10-7-5(8)3-2-4-6(7)9/h2-4H,9H2,1H3
InChIKeyZLODWCIXZJMLJL-UHFFFAOYSA-N
SMILESC1(N)=CC=CC(Br)=C1OC
Safety Information
RIDADR UN 2810 6.1/PG III
HazardClass 6.1
PackingGroup III
HS Code 2922290090
MSDS Information
3-bromo-2-methoxyaniline Usage And Synthesis
Synthesis
1-Bromo-2-methoxy-3-nitro-benzene

98775-19-0

3-bromo-2-methoxyaniline

116557-46-1

The general procedure for the synthesis of 3-bromo-2-methoxyaniline from 2-bromo-6-nitroanisole was as follows: 1-bromo-2-methoxy-3-nitrobenzene (20.1 g, 86.6 mmol) was heated to 80 °C with iron powder (33.4 g, 598 mmol) in a solvent mixture of acetic acid/water (1:1, 600 mL). After the reaction lasted for 1.5 h, the mixture was cooled to room temperature and filtered. The filtered solid was washed several times with ethyl acetate and water. The organic layers were combined, washed with saturated aqueous NaHCO3, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography (eluent: petroleum ether/ethyl acetate = 20:1 to 10:1) to afford 3-bromo-2-methoxyaniline as a yellow solid (17.4 g, 99% yield).1H-NMR (300 MHz, DMSO-d6) δ (ppm): 3.66 (s, 3H), 5.23 (s, 2H), 6.64-6.76 (m, 1H). 3H).

References[1] Patent: EP2987787, 2016, A1. Location in patent: Paragraph 0131
[2] Patent: WO2014/74661, 2014, A1. Location in patent: Paragraph 00173
[3] Patent: US2014/296229, 2014, A1. Location in patent: Paragraph 0258; 0259
[4] Patent: WO2014/154760, 2014, A1. Location in patent: Page/Page column 55-56
[5] Patent: WO2018/75937, 2018, A1. Location in patent: Paragraph 00487; 00495; 00496
3-bromo-2-methoxyaniline Preparation Products And Raw materials
Raw materials2-Bromo-6-nitrophenol-->1-Bromo-2-methoxy-3-nitro-benzene-->Methanol-->2-Amino-6-bromophenol-->Iodomethane-->Acetic acid-->Iron-->Water
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