tert-Butyl 3-aminopyrrolidine-1-carboxylate 2-hydroxypropane-1,2,3-tricarboxylate

95%

Reagent Code: #145938
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CAS Number 1310278-53-5

science Other reagents with same CAS 1310278-53-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 378.38 g/mol
Formula C₁₅H₂₆N₂O₉
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and chiral building blocks. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and receptor agonists due to the structural features of the pyrrolidine ring. The carboxylate salt form enhances stability and solubility, making it suitable for use in aqueous reaction conditions. Also utilized in the manufacture of specialty chemicals requiring enantiomerically pure amines.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,010.00
inventory 5g
10-20 days ฿3,410.00
inventory 10g
10-20 days ฿5,870.00

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tert-Butyl 3-aminopyrrolidine-1-carboxylate 2-hydroxypropane-1,2,3-tricarboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and chiral building blocks. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and receptor agonists due to the structural features of the pyrrolidine ring. The carboxylate salt form enhances stability and solubility, making it suitable for use in aqueous reaction conditions. Also utilized in the manu

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and chiral building blocks. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and receptor agonists due to the structural features of the pyrrolidine ring. The carboxylate salt form enhances stability and solubility, making it suitable for use in aqueous reaction conditions. Also utilized in the manufacture of specialty chemicals requiring enantiomerically pure amines.

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