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Home  > [1,1'-Biphenyl]-4-pentanoic acid, γ-[[(1,1-dimethylethoxy)carbonyl]amino]-α-methyl-, (αS,γR)-

AA04991

1012341-54-6 | [1,1'-Biphenyl]-4-pentanoic acid, γ-[[(1,1-dimethylethoxy)carbonyl]amino]-α-methyl-, (αS,γR)-

Packsize Purity Availability Price Discounted Price    Quantity
10mg 98% 2 weeks $100.00 $70.00 -   +
25mg 98% 2 weeks $190.00 $133.00 -   +
100mg 98% 2 weeks $426.00 $299.00 -   +
250mg 98% 2 weeks $778.00 $545.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA04991
Chemical Name: [1,1'-Biphenyl]-4-pentanoic acid, γ-[[(1,1-dimethylethoxy)carbonyl]amino]-α-methyl-, (αS,γR)-
CAS Number: 1012341-54-6
Molecular Formula: C23H29NO4
Molecular Weight: 383.4807
MDL Number: MFCD28386954
SMILES: C[C@H](C(=O)O)C[C@H](Cc1ccc(cc1)c1ccccc1)NC(=O)OC(C)(C)C

 

Upstream Synthesis Route
  • In chemical synthesis, (αS,​γR)​-γ-​[[(1,​1-​Dimethylethoxy)​carbonyl]​amino]​-​α-​methyl-​[1,​1'-​biphenyl]​-​4-​pentanoic Acid, often referred to simply as $name$, plays a crucial role as a chiral building block. Its unique structure containing both a biphenyl moiety and a pentanoic acid group allows $name$ to be utilized in the development of complex molecules with defined stereochemistry. By incorporating $name$ into chemical reactions, researchers can introduce specific chirality into their target compounds, enabling the creation of enantioenriched products with high levels of selectivity. This versatile compound serves as a valuable tool in the synthesis of pharmaceuticals, natural products, and other fine chemicals that require precise control over stereochemistry for optimal biological activity or functional properties.
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