tert-butylN-(4-nitroanilino)carbamate

96%

Reagent Code: #220281
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CAS Number 92491-67-3

science Other reagents with same CAS 92491-67-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.25 g/mol
Formula C₁₁H₁₅N₃O₄
badge Registry Numbers
MDL Number MFCD01320511
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a Boc-protected form of 1-(4-nitrophenyl)hydrazine, allowing selective reactions at other functional sites without interference from the hydrazine group. The tert-butyloxycarbonyl (Boc) protection enables easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the development of dyes, polymers, and bioactive molecules where controlled hydrazine reactivity is required.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,800.00
inventory 5g
10-20 days ฿20,110.00
tert-butylN-(4-nitroanilino)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a Boc-protected form of 1-(4-nitrophenyl)hydrazine, allowing selective reactions at other functional sites without interference from the hydrazine group. The tert-butyloxycarbonyl (Boc) protection enables easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the development of dyes, polymers, and bioactive molecules whe

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a Boc-protected form of 1-(4-nitrophenyl)hydrazine, allowing selective reactions at other functional sites without interference from the hydrazine group. The tert-butyloxycarbonyl (Boc) protection enables easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the development of dyes, polymers, and bioactive molecules where controlled hydrazine reactivity is required.

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