logo
Home  > Life Science  > Amino acids  > Amino acid derivatives  > (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid

AA17944

1172579-62-2 | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $35.00 $25.00 -   +
250mg 98% in stock $52.00 $37.00 -   +
1g 98% in stock $127.00 $89.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA17944
Chemical Name: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid
CAS Number: 1172579-62-2
Molecular Formula: C22H25NO4
Molecular Weight: 367.4382
MDL Number: MFCD27952009
SMILES: OC(=O)[C@H](C(C)(C)C)N(C(=O)OCC1c2ccccc2-c2c1cccc2)C

 

Computed Properties
Complexity: 533  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 27  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 6  
XLogP3: 4.6  

 

 

Upstream Synthesis Route
  • (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid, commonly referred to as $name$, plays a crucial role in chemical synthesis as a versatile chiral building block. Chemists utilize this compound for its ability to impart chirality into various synthetic pathways, particularly in the production of pharmaceuticals and fine chemicals.Its unique structure allows for precise control over stereochemistry, making it a valuable tool in asymmetric synthesis. By incorporating $name$ into reactions, chemists can selectively generate enantiomerically pure products, which is essential for the development of pharmaceuticals with specific biological activities and minimal side effects.Furthermore, (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid serves as a key intermediate in the synthesis of complex molecules, providing a strategic entry point for the construction of intricate chemical frameworks. Its presence in synthetic routes enables the efficient preparation of chiral compounds with high levels of stereocontrol, facilitating the development of new drug candidates and other biologically active substances.Overall, $name$ is a valuable asset in the toolkit of synthetic chemists, offering precise chiral control and enabling the production of diverse molecules with tailored properties and activities. Its application in chemical synthesis paves the way for the creation of innovative compounds that have the potential to impact various industries, from pharmaceuticals to materials science.
FEATURED PRODUCTS