(S)-Ethyl 2,3-bis((tert-butoxycarbonyl)amino)propanoate

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Reagent Code: #38008
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CAS Number 860033-33-6

science Other reagents with same CAS 860033-33-6

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Weight 332.3926 g/mol
Formula C₁₅H₂₈N₂O₆
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Storage room temperature

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This chemical is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a protected intermediate. It is particularly valuable in organic and medicinal chemistry for constructing complex molecules, as the tert-butoxycarbonyl (Boc) groups provide stability during reactions and can be selectively removed when needed. Its application extends to the development of pharmaceuticals, where it aids in the production of bioactive compounds and drug candidates. Additionally, it is used in research for studying enzyme mechanisms and protein interactions due to its ability to mimic natural amino acid structures.

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inventory 250mg
10-20 days ฿2,142.00

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(S)-Ethyl 2,3-bis((tert-butoxycarbonyl)amino)propanoate
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This chemical is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a protected intermediate. It is particularly valuable in organic and medicinal chemistry for constructing complex molecules, as the tert-butoxycarbonyl (Boc) groups provide stability during reactions and can be selectively removed when needed. Its application extends to the development of pharmaceuticals, where it aids in the production of bioactive compounds and drug candidates. Additionally, it is us

This chemical is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a protected intermediate. It is particularly valuable in organic and medicinal chemistry for constructing complex molecules, as the tert-butoxycarbonyl (Boc) groups provide stability during reactions and can be selectively removed when needed. Its application extends to the development of pharmaceuticals, where it aids in the production of bioactive compounds and drug candidates. Additionally, it is used in research for studying enzyme mechanisms and protein interactions due to its ability to mimic natural amino acid structures.

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