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Home > Encyclopedia > 4-(1-Methylethoxy)benzenamine

4-(1-Methylethoxy)benzenamine

4-(1-Methylethoxy)benzenamine structure

4-(1-Methylethoxy)benzenamine 

structure
  • CAS No:

    7664-66-6

  • Formula:

    C9H13NO

  • Chemical Name:

    4-(1-Methylethoxy)benzenamine

  • Synonyms:

    Benzenamine,4-(1-methylethoxy)-;Aniline,p-isopropoxy-;4-(1-Methylethoxy)benzenamine;4-Isopropoxyaniline;p-Isopropoxyaniline;4-Isopropoxyphenylamine;4-[(1-Methylethyl)oxy]aniline

  • Categories:

    Chemical Reagents  >  Organic Reagents

4-(1-Methylethoxy)benzenamine Basic Attributes

151.21

151.21

231-636-9

DTXSID90227461

2922299090

Characteristics

35.2

2.3

1.0±0.1 g/cm3

244 °C (decomp)

136 °C @ Press: 19 Torr

110.6±13.1 °C

1.535

Safety Information

IRRITANT

36/37/38

26-36/37/39

Xi

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501

H302

|Danger|H301 (33.33%): Toxic if swallowed [Danger Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P310, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P311, P312, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 3 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

4-(1-Methylethoxy)benzenamine Use and Manufacturing

General procedure: These syntheses were carried out in one step as per De Marco et al. [24] Aminophenol (92 mmol) and a suspension of NaH in mineral oil (275 mmol NaH) were suspended in dry DMF (100 mL). The corresponding alkylbromide (137 mmol) was added dropwise and the mixture was then stirred for 24 h at room temperature. The reaction was quenched by adding 400 mL of distilled water and the aqueous layer was extracted with 3 × 150 mL of ethyl acetate. Collected organic layers were dried over anhydrous NaGeneral procedure: A mixture of aryl halide (1 mmol) and sodium alkoxide(3.0 mmol) was refluxed in the presence of 200 mg ofHmCucSILP catalyst in toluene (5 mL) for an appropriatetime as indicated in Table 2. After completion of thereaction, the reaction mixture was filtered and solvent wasevaporated in vacuo to give the crude product, which waspurified by column chromatography over silica gel usinghexane/EtOAc as the eluent.General procedure: A mixture of aryl halide (1 mmol) and sodium alkoxide(3.0 mmol) was refluxed in the presence of 200 mg ofHmCucSILP catalyst in toluene (5 mL) for an appropriatetime as indicated in Table 2. After completion of thereaction, the reaction mixture was filtered and solvent wasevaporated in vacuo to give the crude product, which waspurified by column chromatography over silica gel usinghexane/EtOAc as the eluent.General procedure: A mixture of aryl halide (1 mmol) and sodium alkoxide(3.0 mmol) was refluxed in the presence of 200 mg ofHmCucSILP catalyst in toluene (5 mL) for an appropriatetime as indicated in Table 2. After completion of thereaction, the reaction mixture was filtered and solvent wasevaporated in vacuo to give the crude product, which waspurified by column chromatography over silica gel usinghexane/EtOAc as the eluent.

Computed Properties

Molecular Weight:151.21
XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:151.099714038
Monoisotopic Mass:151.099714038
Topological Polar Surface Area:35.2
Heavy Atom Count:11
Complexity:106
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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