Racemic-(3aR,4R,6aS)-tert-butyl 4-(aminomethyl)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate

95%

Reagent Code: #87821
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CAS Number 1251012-52-8

science Other reagents with same CAS 1251012-52-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.35 g/mol
Formula C₁₃H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD12198694
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those targeting therapeutic applications. Its structure, featuring both an aminomethyl group and a tert-butyl carbamate moiety, makes it a valuable building block for the development of pharmaceutical agents. Researchers often employ it in the design and synthesis of compounds that interact with biological targets, such as enzymes or receptors, due to its potential to introduce specific functional groups into drug candidates. Additionally, its stereochemistry allows for the exploration of chiral compounds, which is crucial in optimizing the efficacy and selectivity of potential drugs. Overall, it serves as a versatile scaffold in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿3,150.00
inventory 5mg
10-20 days ฿5,445.00

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Racemic-(3aR,4R,6aS)-tert-butyl 4-(aminomethyl)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those targeting therapeutic applications. Its structure, featuring both an aminomethyl group and a tert-butyl carbamate moiety, makes it a valuable building block for the development of pharmaceutical agents. Researchers often employ it in the design and synthesis of compounds that interact with biological targets, such as enzymes or receptors, due to its pot

This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those targeting therapeutic applications. Its structure, featuring both an aminomethyl group and a tert-butyl carbamate moiety, makes it a valuable building block for the development of pharmaceutical agents. Researchers often employ it in the design and synthesis of compounds that interact with biological targets, such as enzymes or receptors, due to its potential to introduce specific functional groups into drug candidates. Additionally, its stereochemistry allows for the exploration of chiral compounds, which is crucial in optimizing the efficacy and selectivity of potential drugs. Overall, it serves as a versatile scaffold in drug discovery and development processes.

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