2-Chloro-4,5,6-trimethylnicotinonitrile

95%

Reagent Code: #129389
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CAS Number 91591-64-9

science Other reagents with same CAS 91591-64-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.63 g/mol
Formula C₉H₉ClN₂
badge Registry Numbers
MDL Number MFCD18917078
thermostat Physical Properties
Boiling Point 337.8±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.18±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor agonists and antagonists. It serves in the development of drugs targeting neurological disorders such as Alzheimer's, Parkinson's, and schizophrenia. Also employed in agrochemicals for the formulation of novel insecticides due to its structural affinity to nicotinoids. Its nitrile and chloro functionalities allow for versatile chemical modifications, making it valuable in medicinal chemistry research and development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,330.00
inventory 1g
10-20 days ฿12,650.00

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2-Chloro-4,5,6-trimethylnicotinonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor agonists and antagonists. It serves in the development of drugs targeting neurological disorders such as Alzheimer's, Parkinson's, and schizophrenia. Also employed in agrochemicals for the formulation of novel insecticides due to its structural affinity to nicotinoids. Its nitrile and chloro functionalities allow for versatile chemical modifications, making it valuable in medicinal chemist

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor agonists and antagonists. It serves in the development of drugs targeting neurological disorders such as Alzheimer's, Parkinson's, and schizophrenia. Also employed in agrochemicals for the formulation of novel insecticides due to its structural affinity to nicotinoids. Its nitrile and chloro functionalities allow for versatile chemical modifications, making it valuable in medicinal chemistry research and development.

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