(S)-Methyl 2-(benzylamino)-3-methylbutanoate hydrochloride

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Reagent Code: #38185
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CAS Number 177721-72-1

science Other reagents with same CAS 177721-72-1

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Weight 257.7564 g/mol
Formula C₁₃H₂₀ClNO₂
badge Registry Numbers
MDL Number MFCD02684386
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules for drug discovery. Its structure makes it a valuable building block for creating enantiomerically pure compounds, which are crucial in the production of active pharmaceutical ingredients (APIs) with specific therapeutic effects. It is often employed in research focused on amino acid derivatives, where its chiral center plays a key role in achieving desired biological activity. Additionally, it finds application in peptide chemistry for modifying peptide structures to enhance stability or bioavailability. Its use is also seen in the preparation of compounds targeting neurological and metabolic disorders due to its ability to interact with biological systems effectively.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,521.00

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(S)-Methyl 2-(benzylamino)-3-methylbutanoate hydrochloride
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules for drug discovery. Its structure makes it a valuable building block for creating enantiomerically pure compounds, which are crucial in the production of active pharmaceutical ingredients (APIs) with specific therapeutic effects. It is often employed in research focused on amino acid derivatives, where its chiral center plays a key role in achieving desired biological acti

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules for drug discovery. Its structure makes it a valuable building block for creating enantiomerically pure compounds, which are crucial in the production of active pharmaceutical ingredients (APIs) with specific therapeutic effects. It is often employed in research focused on amino acid derivatives, where its chiral center plays a key role in achieving desired biological activity. Additionally, it finds application in peptide chemistry for modifying peptide structures to enhance stability or bioavailability. Its use is also seen in the preparation of compounds targeting neurological and metabolic disorders due to its ability to interact with biological systems effectively.

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