(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-methoxypropanoate

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Reagent Code: #38093
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CAS Number 134167-07-0

science Other reagents with same CAS 134167-07-0

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Weight 233.2600 g/mol
Formula C₁₀H₁₉NO₅
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MDL Number MFCD18837831
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This compound is primarily used in organic synthesis as a chiral building block for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxy ester, makes it valuable in peptide synthesis, particularly for introducing chiral centers or specific amino acid derivatives. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization. Additionally, the methoxy ester moiety can be hydrolyzed or transformed into other functional groups, enhancing its versatility in constructing complex molecules. Its application is particularly relevant in the development of drugs targeting neurological disorders, cancer, and infectious diseases, where precise stereochemistry is crucial for efficacy.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,455.00

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(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-methoxypropanoate
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This compound is primarily used in organic synthesis as a chiral building block for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxy ester, makes it valuable in peptide synthesis, particularly for introducing chiral centers or specific amino acid derivatives. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization. Additionally, the methoxy ester moi

This compound is primarily used in organic synthesis as a chiral building block for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxy ester, makes it valuable in peptide synthesis, particularly for introducing chiral centers or specific amino acid derivatives. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization. Additionally, the methoxy ester moiety can be hydrolyzed or transformed into other functional groups, enhancing its versatility in constructing complex molecules. Its application is particularly relevant in the development of drugs targeting neurological disorders, cancer, and infectious diseases, where precise stereochemistry is crucial for efficacy.

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