16,17-Epoxyprogesterone

99%

  • Product Code: 40330
  Alias:    16α,17α-Epoxy progesterone; Woerster oxide; 16,17Alpha-Epoxy progesterone; 16.17a-Epoxy-4-pregnene-3,20-dione; Woller oxide;
  CAS:    1097-51-4
Molecular Weight: 328.45 g./mol Molecular Formula: C₂₁H₂₈O₃
EC Number: 214-147-5 MDL Number: MFCD00055948
Melting Point: 128 to 132ºC Boiling Point: 466.9ºC
Density: 1.18 g/cm3 Storage Condition: room temperature
Product Description: 16,17-Epoxyprogesterone is primarily utilized in the field of steroid chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various steroid hormones and related compounds. Researchers use it to develop and study derivatives with potential therapeutic applications, particularly in the areas of endocrinology and hormone regulation. Its epoxy group makes it a valuable building block for modifying steroid structures, enabling the creation of compounds with specific biological activities. Additionally, it has been explored in the context of anti-inflammatory and anti-cancer research due to its structural similarity to bioactive steroids. Its role in these applications highlights its importance in advancing medicinal chemistry and drug discovery.
Product Specification:
Test Specification
Purity 98.5 100%
Appearance White Powder Crystal
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $25.62
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5.000 10-20 days $50.23
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25.000 10-20 days $179.31
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16,17-Epoxyprogesterone
16,17-Epoxyprogesterone is primarily utilized in the field of steroid chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various steroid hormones and related compounds. Researchers use it to develop and study derivatives with potential therapeutic applications, particularly in the areas of endocrinology and hormone regulation. Its epoxy group makes it a valuable building block for modifying steroid structures, enabling the creation of compounds with specific biological activities. Additionally, it has been explored in the context of anti-inflammatory and anti-cancer research due to its structural similarity to bioactive steroids. Its role in these applications highlights its importance in advancing medicinal chemistry and drug discovery.
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