Benzonitrile, 4-[[(2-chlorophenyl)methyl]amino]-

97%

Reagent Code: #141818
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CAS Number 950060-73-8

science Other reagents with same CAS 950060-73-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.7035 g/mol
Formula C₁₄H₁₁ClN₂
thermostat Physical Properties
Boiling Point 406.7±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.24±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure, featuring a benzonitrile core with an aromatic amine substituent, supports the development of bioactive molecules, particularly in the creation of herbicides and plant growth regulators. The compound’s aromatic ring, nitrile, and amine functionalities enable coupling reactions, reductions of the nitrile group, and other functional group transformations, making it valuable in medicinal chemistry for building more complex molecules. It also serves in research settings for developing novel organic compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿32,000.00

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Benzonitrile, 4-[[(2-chlorophenyl)methyl]amino]-
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure, featuring a benzonitrile core with an aromatic amine substituent, supports the development of bioactive molecules, particularly in the creation of herbicides and plant growth regulators. The compound’s aromatic ring, nitrile, and amine functionalities enable coupling reactions, reductions of the nitrile group, and other functional group transformations, making it valuable in medicinal chemistry for buildi
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure, featuring a benzonitrile core with an aromatic amine substituent, supports the development of bioactive molecules, particularly in the creation of herbicides and plant growth regulators. The compound’s aromatic ring, nitrile, and amine functionalities enable coupling reactions, reductions of the nitrile group, and other functional group transformations, making it valuable in medicinal chemistry for building more complex molecules. It also serves in research settings for developing novel organic compounds with potential biological activity.
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