(3S,4S)-tert-Butyl 3-amino-4-methoxypyrrolidine-1-carboxylate

95%

Reagent Code: #36783
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CAS Number 1001635-01-3

science Other reagents with same CAS 1001635-01-3

blur_circular Chemical Specifications

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Weight 216.2800 g/mol
Formula C₁₀H₂₀N₂O₃
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MDL Number MFCD09040597
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description Product Description

This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring both amino and methoxy functional groups, makes it a valuable building block for developing drugs, particularly those targeting neurological and cardiovascular diseases. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in enhancing the efficacy and specificity of the final drug product. Additionally, its tert-butyl carbamate group provides stability during synthetic processes, making it a preferred choice in multi-step organic synthesis.

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inventory 100mg
10-20 days ฿5,715.00

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(3S,4S)-tert-Butyl 3-amino-4-methoxypyrrolidine-1-carboxylate
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This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring both amino and methoxy functional groups, makes it a valuable building block for developing drugs, particularly those targeting neurological and cardiovascular diseases. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in enhancing the efficacy and specificity of the final drug product. Ad
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring both amino and methoxy functional groups, makes it a valuable building block for developing drugs, particularly those targeting neurological and cardiovascular diseases. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in enhancing the efficacy and specificity of the final drug product. Additionally, its tert-butyl carbamate group provides stability during synthetic processes, making it a preferred choice in multi-step organic synthesis.
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