1-Benzyloxy-4-Nitrobenzene

≥98%

Reagent Code: #147112
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CAS Number 1145-76-2

science Other reagents with same CAS 1145-76-2

blur_circular Chemical Specifications

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Weight 229.23 g/mol
Formula C₁₃H₁₁NO₃
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected form of hydroquinone in multi-step reactions where selective functionalization is required. The benzyloxy group can be removed under mild conditions, allowing for controlled deprotection in the synthesis of complex molecules. Also employed in the development of dyes and functional materials due to its nitro group’s electron-withdrawing properties and aromatic stability.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿680.00
inventory 25g
10-20 days ฿2,190.00
inventory 50g
10-20 days ฿3,740.00
inventory 100g
10-20 days ฿4,760.00
inventory 500g
10-20 days ฿20,590.00

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1-Benzyloxy-4-Nitrobenzene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected form of hydroquinone in multi-step reactions where selective functionalization is required. The benzyloxy group can be removed under mild conditions, allowing for controlled deprotection in the synthesis of complex molecules. Also employed in the development of dyes and functional materials due to its nitro group’s electron-withdrawing properties and aromatic stabil

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protected form of hydroquinone in multi-step reactions where selective functionalization is required. The benzyloxy group can be removed under mild conditions, allowing for controlled deprotection in the synthesis of complex molecules. Also employed in the development of dyes and functional materials due to its nitro group’s electron-withdrawing properties and aromatic stability.

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