methyl isoquinoline-4-carboxylate

95%

  • Product Code: 106669
  CAS:    20317-40-2
Molecular Weight: 187.2 g./mol Molecular Formula: C₁₁H₉NO₂
EC Number: MDL Number:
Melting Point: 82℃ Boiling Point: 315.263°C at 760 mmHg
Density: 1.210±0.06 g/cm3(Predicted) Storage Condition: 2-8℃
Product Description: Methyl isoquinoline-4-carboxylate is primarily utilized in the field of organic synthesis as a versatile intermediate. It plays a significant role in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. This chemical is often employed in the creation of alkaloid-like structures, which are crucial in drug discovery for treating various diseases. Additionally, it serves as a building block in the preparation of complex organic molecules, contributing to advancements in medicinal chemistry and the production of bioactive compounds. Its application extends to research laboratories where it is used to study reaction mechanisms and develop new synthetic pathways.
Product Specification:
Test Specification
Appearance Yellow To Brown Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days €28.49
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1.000 10-20 days €86.53
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5.000 10-20 days €271.21
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25.000 10-20 days €1,020.46
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methyl isoquinoline-4-carboxylate
Methyl isoquinoline-4-carboxylate is primarily utilized in the field of organic synthesis as a versatile intermediate. It plays a significant role in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. This chemical is often employed in the creation of alkaloid-like structures, which are crucial in drug discovery for treating various diseases. Additionally, it serves as a building block in the preparation of complex organic molecules, contributing to advancements in medicinal chemistry and the production of bioactive compounds. Its application extends to research laboratories where it is used to study reaction mechanisms and develop new synthetic pathways.
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