(3S,4S)-tert-Butyl 3-(benzylamino)-4-hydroxypyrrolidine-1-carboxylate

95%

Reagent Code: #36780
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CAS Number 252574-03-1

science Other reagents with same CAS 252574-03-1

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Weight 292.3734 g/mol
Formula C₁₆H₂₄N₂O₃
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MDL Number MFCD11109734
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description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a pyrrolidine ring and a benzylamino group, makes it valuable for designing molecules that interact with biological targets, such as enzymes or receptors. Additionally, it is employed in the preparation of chiral compounds, leveraging its stereochemistry to achieve high enantioselectivity in asymmetric synthesis. Its tert-butyl ester group also provides stability during chemical reactions, making it a versatile building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,640.00

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(3S,4S)-tert-Butyl 3-(benzylamino)-4-hydroxypyrrolidine-1-carboxylate
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a pyrrolidine ring and a benzylamino group, makes it valuable for designing molecules that interact with biological targets, such as enzymes or receptors. Additionally, it is employed in the preparation of chiral compounds, leveragin

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a pyrrolidine ring and a benzylamino group, makes it valuable for designing molecules that interact with biological targets, such as enzymes or receptors. Additionally, it is employed in the preparation of chiral compounds, leveraging its stereochemistry to achieve high enantioselectivity in asymmetric synthesis. Its tert-butyl ester group also provides stability during chemical reactions, making it a versatile building block in medicinal chemistry.

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