(S)-METHYL 3-(CBZ-AMINO)BUTANOATE

Reagent Code: #38609
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CAS Number 83460-84-8

science Other reagents with same CAS 83460-84-8

blur_circular Chemical Specifications

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Weight 251.28 g/mol
Formula C₁₃H₁₇NO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily used in organic synthesis as an intermediate in the production of more complex molecules. It serves as a building block in the preparation of pharmaceuticals, particularly in the synthesis of chiral compounds where the (S)-configuration is crucial for biological activity. The CBZ (carbobenzyloxy) protecting group helps in safeguarding the amine functionality during chemical reactions, allowing for selective transformations. It is often employed in peptide synthesis and the development of active pharmaceutical ingredients (APIs) that require specific stereochemistry. Additionally, it finds application in research laboratories for studying enzymatic processes and developing novel drug candidates.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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(S)-METHYL 3-(CBZ-AMINO)BUTANOATE
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This compound is primarily used in organic synthesis as an intermediate in the production of more complex molecules. It serves as a building block in the preparation of pharmaceuticals, particularly in the synthesis of chiral compounds where the (S)-configuration is crucial for biological activity. The CBZ (carbobenzyloxy) protecting group helps in safeguarding the amine functionality during chemical reactions, allowing for selective transformations. It is often employed in peptide synthesis and the deve

This compound is primarily used in organic synthesis as an intermediate in the production of more complex molecules. It serves as a building block in the preparation of pharmaceuticals, particularly in the synthesis of chiral compounds where the (S)-configuration is crucial for biological activity. The CBZ (carbobenzyloxy) protecting group helps in safeguarding the amine functionality during chemical reactions, allowing for selective transformations. It is often employed in peptide synthesis and the development of active pharmaceutical ingredients (APIs) that require specific stereochemistry. Additionally, it finds application in research laboratories for studying enzymatic processes and developing novel drug candidates.

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