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4-CHLORO-2-PHENYLQUINAZOLINE

4-CHLORO-2-PHENYLQUINAZOLINE Structure
4-CHLORO-2-PHENYLQUINAZOLINE
  • CAS No.6484-25-9
  • Chemical Name:4-CHLORO-2-PHENYLQUINAZOLINE
  • CBNumber:CB6137584
  • Molecular Formula:C14H9ClN2
  • Formula Weight:240.69
  • MOL File:6484-25-9.mol
4-CHLORO-2-PHENYLQUINAZOLINE Property
  • Melting point 124-126 °C(lit.)
  • Boiling point 383.11°C (rough estimate)
  • Density 1.285
  • refractive index 1.5749 (estimate)
  • storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
  • pka 0.67±0.30(Predicted)
  • form Crystalline Powder
  • color Slightly yellow to yellow
  • InChIKey OBHKONRNYCDRKM-UHFFFAOYSA-N
  • CAS DataBase Reference 6484-25-9(CAS DataBase Reference)
  • FDA UNII 2QRD56Y64F
  • UNSPSC Code 12352100
  • NACRES NA.22
Safety
  • Hazard Codes  :Xi
  • Risk Statements  :36/37/38
  • Safety Statements  :37/39-26
  • WGK Germany  :3
  • HS Code  :29339980
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H315-H319-H335
  • Precautionary statements P261-P305+P351+P338
4-CHLORO-2-PHENYLQUINAZOLINE Price More Price(1)
  • Brand: Sigma-Aldrich(India)
  • Product number: 162434
  • Product name : 4-Chloro-2-phenylquinazoline
  • Purity: 97%
  • Packaging: 5G
  • Price: ₹4284.6
  • Updated: 2022/06/14
  • Buy: Buy

4-CHLORO-2-PHENYLQUINAZOLINE Chemical Properties,Usage,Production

  • Chemical Properties slightly yellow to yellow crystalline powder
  • Uses Reactant involved in the synthesis of biologically active molecules including:
    • Nitrotriazole amines or nitroimidazole amines for use as antitrypanosomal activity and mammalian cytotoxicity
    • Quinazoline-containing piperazinylpyrimidine derivatives with antitumor activity
    • Quinazoline substituted cyclopentane as HCV NS3/4A protease inhibitors
    • Quinazolines with antibacterial and antitumor activity
    • Aurora inhibitor MK-0457

    Reactant involved in Suzuki-Miyaura cross-coupling and catalyst-free / base-free water promoted nucleophilic aromatic substitution
  • Uses 4-Chloro-2-phenylquinazoline can be involved in the synthesis of biologically active molecules including: Nitrotriazole amines or nitroimidazole amines for use as antitrypanosomal activity and mammalian cytotoxicity.
  • Synthesis Reference(s) Journal of the American Chemical Society, 68, p. 1299, 1946 DOI: 10.1021/ja01211a055
4-CHLORO-2-PHENYLQUINAZOLINE Preparation Products And Raw materials
Raw materials
Preparation Products
4-CHLORO-2-PHENYLQUINAZOLINE Suppliers
Global(122)Suppliers
  • Supplier：
    Alchem Pharmtech,Inc.
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  • Supplier：
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  • Supplier：
    Richest Group Ltd
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  • Country：CHINA
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4-CHLORO-2-PHENYLQUINAZOLINE Spectrum
6484-25-9, 4-CHLORO-2-PHENYLQUINAZOLINERelated Search:
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  • 4-CHLORO-2-PHENYLQUINAZOLINE OR AM-ex-OL
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  • 4-CHLORO-2-PHENYLQUINAZOLINE
  • AM-EX-OL(R)
  • AKOS 93518

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