tert-butyl 1-benzyl-3-(hydroxymethyl)pyrrolidin-3-ylcarbamate

95%

Reagent Code: #40221
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CAS Number 475469-14-8

science Other reagents with same CAS 475469-14-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.4100 g/mol
Formula C₁₇H₂₆N₂O₃
badge Registry Numbers
MDL Number MFCD06410561
thermostat Physical Properties
Boiling Point 419.335 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.147g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of biologically active molecules, particularly in the synthesis of compounds targeting neurological disorders. Its structure, featuring a pyrrolidine ring and a benzyl group, makes it valuable for designing inhibitors of enzymes or receptors involved in disease pathways. Additionally, the presence of the tert-butyl carbamate group enhances its stability, making it suitable for use in multi-step synthetic processes. Researchers also explore its potential in creating prodrugs or modifying drug delivery systems to improve bioavailability and therapeutic efficacy.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,580.00

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tert-butyl 1-benzyl-3-(hydroxymethyl)pyrrolidin-3-ylcarbamate
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of biologically active molecules, particularly in the synthesis of compounds targeting neurological disorders. Its structure, featuring a pyrrolidine ring and a benzyl group, makes it valuable for designing inhibitors of enzymes or receptors involved in disease pathways. Additionally, the presence of the tert-butyl carbamate group enhances its stability, ma

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of biologically active molecules, particularly in the synthesis of compounds targeting neurological disorders. Its structure, featuring a pyrrolidine ring and a benzyl group, makes it valuable for designing inhibitors of enzymes or receptors involved in disease pathways. Additionally, the presence of the tert-butyl carbamate group enhances its stability, making it suitable for use in multi-step synthetic processes. Researchers also explore its potential in creating prodrugs or modifying drug delivery systems to improve bioavailability and therapeutic efficacy.

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