4-Benzoylbenzonitrile
≥95%
Reagent
Code: #119649
CAS Number
1503-49-7
blur_circular Chemical Specifications
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Molecular Information
Weight
207.23 g/mol
Formula
C₁₄H₉NO
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Registry Numbers
MDL Number
MFCD00016382
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Physical Properties
Boiling Point
377°C at 760 mmHg
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Storage & Handling
Density
1.19g/cm3
Storage
Room temperature, dry and sealed
description Product Description
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its benzoyl and nitrile functional groups make it valuable for constructing complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Additionally, it is employed in the synthesis of photoinitiators for UV-curable coatings and inks, enhancing their efficiency and performance. In materials science, it contributes to the creation of advanced polymers and resins with specific optical or mechanical properties. Its versatility in chemical reactions also makes it a useful reagent in academic and industrial research for exploring new synthetic pathways.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Light Yellow Powder |
Purity (%) | 94.5-100% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
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4-Benzoylbenzonitrile
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its benzoyl and nitrile functional groups make it valuable for constructing complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Additionally, it is employed in the synthesis of photoinitiators for UV-curable coatings and inks, enhancing their efficiency and performance. In materials science, it contributes to the creation of advanced polymers and resins with specific optical or mechanical properties. Its versatility in chemical reactions also makes it a useful reagent in academic and industrial research for exploring new synthetic pathways.
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