(R)-Methyl 2-((Tert-Butoxycarbonyl)Amino)-3-Chloropropanoate

98%

Reagent Code: #231588
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CAS Number 651035-84-6

science Other reagents with same CAS 651035-84-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.68 g/mol
Formula C₉H₁₆ClNO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of beta-amino acid derivatives and peptidomimetics. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating active pharmaceutical ingredients (APIs) with high enantiomeric purity. Commonly employed in the preparation of protease inhibitors and other biologically active molecules where control of molecular configuration is critical. The Boc-protected amine and ester functionalities enable stepwise deprotection and coupling reactions, facilitating its incorporation into complex organic structures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,930.00
(R)-Methyl 2-((Tert-Butoxycarbonyl)Amino)-3-Chloropropanoate
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of beta-amino acid derivatives and peptidomimetics. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating active pharmaceutical ingredients (APIs) with high enantiomeric purity. Commonly employed in the preparation of protease inhibitors and other biologically active molecules where control of molecular configuration is critical. The Boc-pr

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of beta-amino acid derivatives and peptidomimetics. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating active pharmaceutical ingredients (APIs) with high enantiomeric purity. Commonly employed in the preparation of protease inhibitors and other biologically active molecules where control of molecular configuration is critical. The Boc-protected amine and ester functionalities enable stepwise deprotection and coupling reactions, facilitating its incorporation into complex organic structures.

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