4-Bromo-3,5-dimethylisoxazole

>98.0%(GC)

  • Product Code: 119323
  Alias:    3,5-Dimethyl-4-bromoisoxazole 4-Bromo-3,5-dimethylethyl ester
  CAS:    10558-25-5
Molecular Weight: 176.01 g./mol Molecular Formula: C₅H₆BrNO
EC Number: MDL Number: MFCD00068187
Melting Point: Boiling Point: 176 °C(lit.)
Density: 1.478 g/mL at 25 °C(lit.) Storage Condition: 2~8°C
Product Description: Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the development of pharmaceuticals and agrochemicals. Its structure allows for the introduction of bromine into more complex molecules, facilitating the creation of compounds with potential biological activity. In medicinal chemistry, it serves as a building block for the synthesis of various drugs, particularly those targeting neurological and infectious diseases. Additionally, it is employed in research settings to study chemical reactions and mechanisms involving halogenated heterocycles, aiding in the discovery of new chemical entities.
Product Specification:
Test Specification
Purity (GC) 98
Refractive Index N20/D 1.488-1.492
Specific Gravity (20/20 Degree Celsius) 1.539-1.544
Appearance Colorless To Brown Liquid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿260.00
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5.000 10-20 days ฿660.00
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25.000 10-20 days ฿1,940.00
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-
100.000 10-20 days ฿4,720.00
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4-Bromo-3,5-dimethylisoxazole
Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the development of pharmaceuticals and agrochemicals. Its structure allows for the introduction of bromine into more complex molecules, facilitating the creation of compounds with potential biological activity. In medicinal chemistry, it serves as a building block for the synthesis of various drugs, particularly those targeting neurological and infectious diseases. Additionally, it is employed in research settings to study chemical reactions and mechanisms involving halogenated heterocycles, aiding in the discovery of new chemical entities.
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