N-ISOPROPYLANILINE (768-52-5)

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Suppliers

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  5 g
  $13.00

  25 g
  $40.00

Most-cited Publications

• MOLECULAR ADDITION COMPOUNDS. 11. N-ETHYL-N-ISOPROPYLANILINE-BORANE, A SUPERIOR REAGENT FOR HYDROBORATIONS AND REDUCTIONS (Journal of Organic Chemistry, 1998)
• Spin-Crossover Hysteresis of [FeII(LHiPr)2(NCS)2] (LHiPr = N-2-Pyridylmethylene-4-Isopropylaniline) Accompanied by Isopropyl Conformation Isomerism (Magnetochemistry, 2015)
• Method for producing 2,4-difluoro -n- isopropylaniline (2001)
• [Determination of N-isopropylaniline in workplace air by high-performance liquid chromatography]. (2015)
• [Gas chromatography for determination of N-isopropylaniline in workplace atmosphere]. (2015)
• X-Ray Photoelectron Spectroscopy and X-Ray Diffraction Studies on Deactivation of Barium Promoted Copper Chromium Oxide Catalyst Used in the Synthesis of N-Isopropylaniline (Oriental journal of chemistry, 2001)

Safety

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  Predict GHS Hazards for Any Chemical in silico.
  Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more.
• H227: Combustible liquid
  Warning Flammable liquids - Category 4
• H313: May be harmful in contact with skin
  Acute toxicity, dermal - Category 5
• H332: Harmful if inhaled
  Warning Acute toxicity, inhalation - Category 4
• H361: Suspected of damaging fertility or the unborn child
  Warning Reproductive toxicity - Category 2

Trends

Alternate Names

• N-isopropylaniline hydrochloride
• SMILES
  CC(C)NC1=CC=CC=C1
• InChIKey
  FRCFWPVMFJMNDP-UHFFFAOYSA-N

External Links

• Pubchem - N-ISOPROPYLANILINE
• Wikipedia - N-isopropyl aniline

Synthesis

ANILINE  +  2-CHLOROPROPANE (Alkylation of primary amines)

Synthesis of N-ISOPROPYLANILINE ›

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N-ISOPROPYLANILINE

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