2-(4-((tert-Butoxycarbonyl)amino)-2-nitrophenyl)acetic acid

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Reagent Code: #41543
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CAS Number 512180-63-1

science Other reagents with same CAS 512180-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.2759 g/mol
Formula C₁₃H₁₆N₂O₆
badge Registry Numbers
MDL Number MFCD08236844
thermostat Physical Properties
Boiling Point 403.5 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.36g/cm3
Storage room temperature

description Product Description

Used in organic synthesis as an intermediate for the preparation of pharmaceuticals and bioactive compounds. This molecule features a tert-butoxycarbonyl (Boc)-protected aniline moiety on a 2-nitrophenylacetic acid scaffold, enabling selective deprotection and precise construction of complex molecules, particularly in peptide analogs and modified amino acid derivatives. The nitro and aromatic groups facilitate further derivatizations, such as reductions or cyclizations. It is also applicable in dye and pigment synthesis due to its chromophoric potential. Its balanced stability and reactivity make it versatile for research and industrial use.

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inventory 100mg
10-20 days ฿7,101.00

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2-(4-((tert-Butoxycarbonyl)amino)-2-nitrophenyl)acetic acid
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Used in organic synthesis as an intermediate for the preparation of pharmaceuticals and bioactive compounds. This molecule features a tert-butoxycarbonyl (Boc)-protected aniline moiety on a 2-nitrophenylacetic acid scaffold, enabling selective deprotection and precise construction of complex molecules, particularly in peptide analogs and modified amino acid derivatives. The nitro and aromatic groups facilitate further derivatizations, such as reductions or cyclizations. It is also applicable in dye and p

Used in organic synthesis as an intermediate for the preparation of pharmaceuticals and bioactive compounds. This molecule features a tert-butoxycarbonyl (Boc)-protected aniline moiety on a 2-nitrophenylacetic acid scaffold, enabling selective deprotection and precise construction of complex molecules, particularly in peptide analogs and modified amino acid derivatives. The nitro and aromatic groups facilitate further derivatizations, such as reductions or cyclizations. It is also applicable in dye and pigment synthesis due to its chromophoric potential. Its balanced stability and reactivity make it versatile for research and industrial use.

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