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105590-97-4

H-GLU(OBZL)-OTBU HCL

Catalog#: AR008UY7  |   CAS#: 105590-97-4  |   MDL#: MFCD00038897  |   MF: C16H24ClNO4  |   MW: 329.8191

Packsize Purity Price Availability Quantity
1g 97% $4.00 Global Stock Buy Now Add To Cart
5g 97% $10.00 Global Stock Buy Now Add To Cart
10g 97% $15.00 Global Stock Buy Now Add To Cart
25g 97% $37.00 Global Stock Buy Now Add To Cart
100g 97% $140.00 Global Stock Buy Now Add To Cart
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Catalog Number AR008UY7
Chemical Name H-GLU(OBZL)-OTBU HCL
CAS Number 105590-97-4
Molecular Formula C16H24ClNO4
Molecular Weight 329.8191
MDL Number MFCD00038897
SMILES N[C@H](C(=O)OC(C)(C)C)CCC(=O)OCc1ccccc1.Cl

(S)-5-Benzyl 1-tert-butyl 2-aminopentanedioate hydrochloride is a versatile compound commonly used in chemical synthesis. In synthesis applications, this compound serves as a valuable chiral building block due to its unique structural properties. It can be employed as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.One notable application of (S)-5-Benzyl 1-tert-butyl 2-aminopentanedioate hydrochloride is in the enantioselective synthesis of biologically active compounds. By utilizing this compound as a chiral auxiliary or ligand, chemists can facilitate the creation of stereochemically complex molecules with high enantiomeric purity. This compound's stereochemistry plays a crucial role in directing the formation of desired stereoisomers, enabling the precise control over the spatial arrangement of atoms in the target molecules.Moreover, (S)-5-Benzyl 1-tert-butyl 2-aminopentanedioate hydrochloride can act as a catalyst or reagent in asymmetric synthesis reactions, promoting the efficient construction of chiral centers in organic molecules. Its presence in a reaction mixture can lead to improved yields, selectivity, and overall efficiency in the synthesis of valuable compounds. Chemists often rely on this compound to access enantiomerically pure building blocks that are essential for the preparation of complex molecules with specific biological or pharmacological activities.Overall, the application of (S)-5-Benzyl 1-tert-butyl 2-aminopentanedioate hydrochloride in chemical synthesis highlights its significance as a versatile tool for accessing chiral compounds with tailored stereochemical properties. By leveraging its chiral nature and reactivity, researchers can advance the development of novel materials and pharmaceuticals with enhanced therapeutic potential.
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