methyl4-((tert-butoxycarbonyl)amino)-2,6-dichlorobenzoate

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Reagent Code: #124621
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CAS Number 409127-35-1

science Other reagents with same CAS 409127-35-1

blur_circular Chemical Specifications

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Weight 320.17 g/mol
Formula C₁₃H₁₅Cl₂NO₄
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description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps protect amino groups during reactions. The dichlorobenzoate moiety contributes to its utility in creating complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Additionally, it finds applications in research settings for studying chemical reactions and designing novel compounds with potential therapeutic or agricultural benefits.

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inventory 100mg
10-20 days ฿18,000.00

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methyl4-((tert-butoxycarbonyl)amino)-2,6-dichlorobenzoate
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps protect amino groups during reactions. The dichlorobenzoate moiety contributes to its utility in creating complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Additionally, it finds applications in resear

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps protect amino groups during reactions. The dichlorobenzoate moiety contributes to its utility in creating complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Additionally, it finds applications in research settings for studying chemical reactions and designing novel compounds with potential therapeutic or agricultural benefits.

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