3-Isobutoxy-4-nitrobenzoic acid

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Reagent Code: #130376
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CAS Number 859034-50-7

science Other reagents with same CAS 859034-50-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.22 g/mol
Formula C₁₁H₁₃NO₅
badge Registry Numbers
MDL Number MFCD14543051
thermostat Physical Properties
Melting Point 193 °C
Boiling Point 414.8±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.274±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of photochromic compounds, particularly in the production of dyes and pigments that change color under UV light. It plays a role in the development of light-sensitive materials for ophthalmic lenses, optical switches, and smart windows. Its nitro and carboxylic acid functional groups allow for further chemical modifications, making it valuable in organic synthesis for pharmaceuticals and agrochemicals. Also utilized in research for developing sensors and molecular switches due to its electron-withdrawing properties and structural stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,110.00
inventory 1g
10-20 days ฿24,560.00

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3-Isobutoxy-4-nitrobenzoic acid
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Used as an intermediate in the synthesis of photochromic compounds, particularly in the production of dyes and pigments that change color under UV light. It plays a role in the development of light-sensitive materials for ophthalmic lenses, optical switches, and smart windows. Its nitro and carboxylic acid functional groups allow for further chemical modifications, making it valuable in organic synthesis for pharmaceuticals and agrochemicals. Also utilized in research for developing sensors and molecular

Used as an intermediate in the synthesis of photochromic compounds, particularly in the production of dyes and pigments that change color under UV light. It plays a role in the development of light-sensitive materials for ophthalmic lenses, optical switches, and smart windows. Its nitro and carboxylic acid functional groups allow for further chemical modifications, making it valuable in organic synthesis for pharmaceuticals and agrochemicals. Also utilized in research for developing sensors and molecular switches due to its electron-withdrawing properties and structural stability.

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