Methyl 3-(((tert-butoxycarbonyl)amino)methyl)benzoate

97%

Reagent Code: #209016
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CAS Number 180863-55-2

science Other reagents with same CAS 180863-55-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.31 g/mol
Formula C₁₄H₁₉NO₄
badge Registry Numbers
MDL Number MFCD14583094
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protected amino groups are required. Its ester and Boc-protected amine functionalities make it valuable in peptide coupling reactions and in building complex molecules through stepwise organic synthesis. Commonly employed in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and inflammatory diseases. Also utilized in research settings for preparing prodrugs and bifunctional linkers in bioconjugation.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,350.00
5g
10-20 days ฿4,480.00
10g
10-20 days ฿6,840.00
25g
10-20 days ฿16,040.00
Methyl 3-(((tert-butoxycarbonyl)amino)methyl)benzoate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protected amino groups are required. Its ester and Boc-protected amine functionalities make it valuable in peptide coupling reactions and in building complex molecules through stepwise organic synthesis. Commonly employed in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and inflammatory diseases. Also util

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protected amino groups are required. Its ester and Boc-protected amine functionalities make it valuable in peptide coupling reactions and in building complex molecules through stepwise organic synthesis. Commonly employed in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and inflammatory diseases. Also utilized in research settings for preparing prodrugs and bifunctional linkers in bioconjugation.

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