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Home  > (3α,4α,8α,9β,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-29-nordaMMara-17(20),24-dien-21-oic Acid

AE22212

1013937-16-0 | (3α,4α,8α,9β,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-29-nordaMMara-17(20),24-dien-21-oic Acid

Packsize Purity Availability Price Discounted Price    Quantity
2.5mg 3 weeks $315.00 $220.00 -   +
10mg 3 weeks $772.00 $540.00 -   +

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Description
Catalog Number: AE22212
Chemical Name: (3α,4α,8α,9β,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-29-nordaMMara-17(20),24-dien-21-oic Acid
CAS Number: 1013937-16-0
Molecular Formula: C31H48O5
Molecular Weight: 500.7098
MDL Number: MFCD00006587
SMILES: CC(=O)O[C@H]1C[C@]2([C@H](/C/1=C(/C(=O)O)\CC/C=C(/C)\C)CC[C@@H]1[C@]2(C)CC[C@@H]2[C@]1(C)CC[C@H]([C@H]2C)O)C

 

Upstream Synthesis Route 
  • The compound (3α,4α,8α,9β,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-29-nordammara-17(20),24-dien-21-oic acid has garnered significant interest in chemical synthesis due to its unique structural features and versatile reactivity. This compound serves as a valuable building block in the synthesis of various complex natural products and pharmaceutical compounds. Its functional groups, including the hydroxy and acetoxy moieties, enable selective chemical transformations that are crucial in the construction of intricate molecular structures. Furthermore, the presence of multiple chiral centers in this compound offers opportunities for stereocontrolled synthesis, making it a valuable tool in asymmetric synthesis strategies.
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