| Identification | More |  [Name]
  4-Bromo-1-naphthylamine |  [CAS]
  2298-07-9 |  [Synonyms]
  1-AMINO-4-BROMONAPHTHALENE 4-BROMO-1-NAPHTHALENAMINE 4-BROMO-1-NAPHTHYLAMINE 1-Amino-4-bromoaphthlalene 1-Naphthalenamine, 4-bromo- 4-BROMO-1-NAPHTHALENYLAMINE 4-Bromo-1-naphtylamine 4-Bromonaphthalene-1-amine |  [EINECS(EC#)]
  218-944-9 |  [Molecular Formula]
  C10H8BrN |  [MDL Number]
  MFCD00004023 |  [Molecular Weight]
  222.08 |  [MOL File]
  2298-07-9.mol |  
 | Chemical Properties | Back Directory |  [Melting point ]
  102-103 °C(lit.) 
 |  [Boiling point ]
  338.4±17.0 °C(Predicted) |  [density ]
  1.563±0.06 g/cm3(Predicted) |  [storage temp. ]
  Keep in dark place,Sealed in dry,Room Temperature |  [form ]
  powder to crystal |  [pka]
  2.93±0.10(Predicted) |  [color ]
  White to Amber to Dark purple |  [InChI]
  InChI=1S/C10H8BrN/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6H,12H2 |  [InChIKey]
  LIUKLAQDPKYBCP-UHFFFAOYSA-N |  [SMILES]
  C1(N)=C2C(C=CC=C2)=C(Br)C=C1 |  [CAS DataBase Reference]
  2298-07-9(CAS DataBase Reference) |  
 | Safety Data | Back Directory |  [Hazard Codes ]
  Xi,Xn |  [Risk Statements ]
  R36/37/38:Irritating to eyes, respiratory system and skin . R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . |  [Safety Statements ]
  S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S37/39:Wear suitable gloves and eye/face protection . S36:Wear suitable protective clothing . |  [WGK Germany ]
  3 
 |  [Hazard Note ]
  Irritant |  [HS Code ]
  29214990 |  
 | Hazard Information | Back Directory |  [Chemical Properties]
  pale purple fibrous powder |  [Uses]
  1-Amino-4-bromonaphthalene is a reagent used in catalytic asymmetric ring opening of meso-epoxides with aromatic amines in water. It can also be used to synthesize of 4-quinolones and quinolone heterocycles. |  [Synthesis]
  4-Bromo-1-naphthylamine is synthesised using 1-(acetylamino)-4-bromonaphthalene as a raw material by chemical reaction. The specific synthesis steps are as follows: The 4-bromo-1-acetamido naphthalene obtained in the first step is dissolved in 100 mL of 95% ethanol, and the mass concentration of 4-bromo-1-acetylaminonaphthalene in the mixed solution is 30%, and the mass concentration is 37% added to the mixed solution. 50mL of concentrated hydrochloric acid, reacted at 80 ° C for 6h, filtered and dried to give 4-bromo-1-naphthylamine.
   |  [References]
  [1] Synthesis,  2004,  # 17,  p. 2809 - 2812 [2] Journal of the Brazilian Chemical Society,  2010,  vol. 21,  # 3,  p. 496 - 501 [3] Journal of the Chinese Chemical Society,  2005,  vol. 52,  # 3,  p. 559 - 562 [4] Synthetic Communications,  2005,  vol. 35,  # 14,  p. 1947 - 1952 [5] Russian Journal of Organic Chemistry,  2007,  vol. 43,  # 9,  p. 1282 - 1284 |  
  
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