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Home  > (R)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-4-methylpentanoic acid

AA07366

1018899-99-4 | (R)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-4-methylpentanoic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $74.00 $52.00 -   +
250mg 98% in stock $123.00 $87.00 -   +
1g 98% in stock $353.00 $248.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA07366
Chemical Name: (R)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-4-methylpentanoic acid
CAS Number: 1018899-99-4
Molecular Formula: C22H25NO4
Molecular Weight: 367.4382
MDL Number: MFCD07372889
SMILES: CC(C[C@@H](C(=O)O)CNC(=O)OCC1c2ccccc2-c2c1cccc2)C

 

Computed Properties
Complexity: 498  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 27  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 8  
XLogP3: 4.3  

 

 

Upstream Synthesis Route
  • The (R)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-4-methylpentanoic acid is a versatile compound widely utilized in chemical synthesis due to its unique properties. In organic synthesis, this particular compound is commonly employed as a chiral building block to introduce asymmetry into molecular structures. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial in pharmaceutical and agrochemical industries where stereochemistry plays a significant role in biological activity. With its distinct structure and functional groups, (R)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-4-methylpentanoic acid serves as a key component in the development of complex molecules and the synthesis of novel chemical entities.
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