logo
Home  > 1-Oxaspiro[2.5]octan-6-ol,5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-,(3R,4S,5S,6R)-

AD66858

108102-51-8 | 1-Oxaspiro[2.5]octan-6-ol,5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-,(3R,4S,5S,6R)-

Packsize Purity Availability Price Discounted Price    Quantity
1mg 98% in stock $228.00 $160.00 -   +
5mg 98% in stock $497.00 $348.00 -   +
10mg 98% in stock $825.00 $578.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD66858
Chemical Name: 1-Oxaspiro[2.5]octan-6-ol,5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-,(3R,4S,5S,6R)-
CAS Number: 108102-51-8
Molecular Formula: C16H26O4
Molecular Weight: 282.37523999999996
MDL Number: MFCD04035560
SMILES: CO[C@@H]1[C@H](O)CC[C@@]2([C@H]1[C@@]1(C)O[C@@H]1C/C=C(\C)/C)CO2

 

Upstream Synthesis Route
  • Fumagillol, a naturally occurring compound derived from the fungus Aspergillus fumigatus, is a valuable resource in chemical synthesis due to its unique properties. In the realm of organic chemistry, Fumagillol has been harnessed for its ability to serve as a versatile building block in the production of various pharmaceuticals and bioactive molecules. Its complex structure and functional groups make it a key ingredient in the synthesis of diverse compounds, ranging from anticancer agents to antimicrobial drugs. By leveraging Fumagillol in chemical reactions, researchers can access new pathways and strategies for creating novel compounds with therapeutic potential. Its significance in chemical synthesis lies in its ability to facilitate the creation of complex molecular structures with precision and efficiency, making it an indispensable tool for drug discovery and development.
FEATURED PRODUCTS