4-Nitrobenzophenone

99%

Reagent Code: #216651
label
Alias 4-Nitrobenzophenone
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CAS Number 1144-74-7

science Other reagents with same CAS 1144-74-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.22 g/mol
Formula C₁₃H₉NO₃
badge Registry Numbers
EC Number 214-542-2
MDL Number MFCD00007354
thermostat Physical Properties
Melting Point 136-138 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and dyes, particularly in the production of certain antihistamines and sunscreen agents. It also serves as a building block in organic synthesis for introducing nitro-substituted aromatic systems. Its photochemical properties make it useful in studies involving photoaffinity labeling to investigate biological binding sites. Additionally, it finds application in the preparation of liquid crystals and other functional materials due to its stable aromatic structure and electron-withdrawing nitro group.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿250.00
5g
10-20 days ฿310.00
25g
10-20 days ฿1,060.00
100g
10-20 days ฿3,750.00
4-Nitrobenzophenone
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Used as an intermediate in the synthesis of pharmaceuticals and dyes, particularly in the production of certain antihistamines and sunscreen agents. It also serves as a building block in organic synthesis for introducing nitro-substituted aromatic systems. Its photochemical properties make it useful in studies involving photoaffinity labeling to investigate biological binding sites. Additionally, it finds application in the preparation of liquid crystals and other functional materials due to its stable a

Used as an intermediate in the synthesis of pharmaceuticals and dyes, particularly in the production of certain antihistamines and sunscreen agents. It also serves as a building block in organic synthesis for introducing nitro-substituted aromatic systems. Its photochemical properties make it useful in studies involving photoaffinity labeling to investigate biological binding sites. Additionally, it finds application in the preparation of liquid crystals and other functional materials due to its stable aromatic structure and electron-withdrawing nitro group.

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