| Identification | More | [Name]
4-Isopropoxyaniline | [CAS]
7664-66-6 | [Synonyms]
4-ISOPROPOXYANILINE
4-ISOPROPOXYBENZENAMINE
4-ISOPROPOXYLANILINE
4-ISOPROPOXY-PHENYLAMINE
4-ISOPROPYLOXYANILINE
AKOS BBB/094
AKOS BC-2569
P-ISOPROPOXYANILINE
TIMTEC-BB SBB010330
4-ISOPROPOXYBENZENAMINE:99+% | [EINECS(EC#)]
231-636-9 | [Molecular Formula]
C9H13NO | [MDL Number]
MFCD00059188 | [Molecular Weight]
151.21 | [MOL File]
7664-66-6.mol |
| Chemical Properties | Back Directory | [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 | [form ]
clear liquid | [pka]
6.15±0.10(Predicted) | [color ]
Colorless to Red to Green | [LogP]
1.620 (est) | [CAS DataBase Reference]
7664-66-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [HazardClass ]
IRRITANT | [HS Code ]
29214200 |
| Hazard Information | Back Directory | [Uses]
4-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]
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, |
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