tert-Butyl 2,4-dichloro-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate

97%

  • Product Code: 115297
  CAS:    916420-27-4
Molecular Weight: 304.17 g./mol Molecular Formula: C₁₂H₁₅Cl₂N₃O₂
EC Number: MDL Number: MFCD09025732
Melting Point: Boiling Point: 423.1°C at 760 mmHg
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the construction of pyridopyrimidine derivatives, which are known for their potential therapeutic applications. Researchers often employ it in the design and synthesis of compounds targeting various diseases, including cancer and inflammatory disorders. Its role as a building block allows for the introduction of specific functional groups, enabling the exploration of structure-activity relationships in drug discovery. Additionally, it may be used in the preparation of small-molecule inhibitors that modulate specific enzymatic pathways, contributing to the development of novel therapeutic agents.
Product Specification:
Test Specification
Appearance White To Yellow Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿780.00
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0.250 10-20 days ฿1,320.00
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1.000 10-20 days ฿2,840.00
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-
5.000 10-20 days ฿9,350.00
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-
tert-Butyl 2,4-dichloro-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the construction of pyridopyrimidine derivatives, which are known for their potential therapeutic applications. Researchers often employ it in the design and synthesis of compounds targeting various diseases, including cancer and inflammatory disorders. Its role as a building block allows for the introduction of specific functional groups, enabling the exploration of structure-activity relationships in drug discovery. Additionally, it may be used in the preparation of small-molecule inhibitors that modulate specific enzymatic pathways, contributing to the development of novel therapeutic agents.
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