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4-Isopropoxyaniline

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CAS:7664-66-6
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CAS:7664-66-6
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:7664-66-6
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4-Isopropoxyaniline manufacturers

  • 4-Isopropoxyaniline
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  • $0.00 / 1kg
  • 2026-03-16
  • CAS:7664-66-6
  • Min. Order: 1kg
  • Purity: 97%
  • Supply Ability: 20 tons
  • 4-Isopropoxyaniline
  • 4-Isopropoxyaniline pictures
  • $1.00 / 1kg
  • 2019-07-06
  • CAS:7664-66-6
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 200kg
4-Isopropoxyaniline Basic information
Product Name:4-Isopropoxyaniline
Synonyms:P-ISOPROPOXYANILINE;4-ISOPROPOXYBENZENAMINE:99+%;4-(propan-2-yloxy)aniline;4-isopropoxyanline;AKOS BC-2569;AKOS BBB/094;4-ISOPROPOXYANILINE;4-ISOPROPOXYBENZENAMINE
CAS:7664-66-6
MF:C9H13NO
MW:151.21
EINECS:231-636-9
Product Categories:Anilines, Aromatic Amines and Nitro Compounds
Mol File:7664-66-6.mol
4-Isopropoxyaniline Structure
4-Isopropoxyaniline Chemical Properties
Melting point 244 °C (decomp)
Boiling point 95°C 0,4mm
density 1.03
refractive index 1.5430-1.5470
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka6.15±0.10(Predicted)
form clear liquid
color Colorless to Red to Green
LogP1.620 (est)
CAS DataBase Reference7664-66-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HazardClass IRRITANT
HS Code 29214200
MSDS Information
4-Isopropoxyaniline Usage And Synthesis
Uses4-Isopropoxyaniline is an aniline derivative used as a raw material or intermediate component in organic synthesis. It can be used in the preparation of pyrimidines and their derivatives. Anilines are toxic to humans and can cause strong skin and eye irritation on contact or ingestion, as well as some damage to the liver and kidneys.
Synthesis
4-Aminophenol

123-30-8

2-Bromopropane

75-26-3

4-Isopropoxyaniline

7664-66-6

GENERAL STEPS: The synthesis was carried out according to the one-step method reported by De Marco et al. 4-Aminophenol (92 mmol) and sodium hydride (suspension in mineral oil, 275 mmol) were added to anhydrous N,N-dimethylformamide (100 mL). Subsequently, 2-bromopropane (137 mmol) was added dropwise and the reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, distilled water (400 mL) was added to quench the reaction and the aqueous phase was extracted with ethyl acetate (3 x 150 mL). The organic layers were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The final product was purified by distillation under reduced pressure.

References[1] Molecules, 2015, vol. 20, # 6, p. 9767 - 9787
[2] Journal of Medicinal Chemistry, 2007, vol. 50, # 20, p. 4898 - 4908
[3] Molecules, 2018, vol. 23, # 7,
4-Isopropoxyaniline Preparation Products And Raw materials
Raw materials4-Aminophenol-->Sodium propan-2-olate-->4-Iodoaniline-->2-Bromopropane-->4-Chloroaniline-->4-Bromoaniline-->Mineral oil-->Sodium hydride-->N,N-Dimethylformamide
Preparation Products2-Bromo-4-isopropoxyaniline
Tag:4-Isopropoxyaniline(7664-66-6) Related Product Information
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