5-Bromo-2-(dimethylamino)nicotinonitrile

95%

Reagent Code: #152312
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CAS Number 1346537-10-7

science Other reagents with same CAS 1346537-10-7

blur_circular Chemical Specifications

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Weight 226.07 g/mol
Formula C₈H₈BrN₃
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MDL Number MFCD19688659
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the formation of complex heterocyclic compounds that are active in biological systems. Commonly employed in medicinal chemistry for constructing nitrogen-containing ring systems. Also utilized in agrochemical research for designing new bioactive molecules. Suitable for coupling reactions in organic synthesis due to the presence of bromine and nitrile functional groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,100.00
inventory 250mg
10-20 days ฿10,360.00
inventory 1g
10-20 days ฿30,280.00

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5-Bromo-2-(dimethylamino)nicotinonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the formation of complex heterocyclic compounds that are active in biological systems. Commonly employed in medicinal chemistry for constructing nitrogen-containing ring systems. Also utilized in agrochemical research for designing new bioactive molecules. Suitable for coupling reactions in organic synthesis due to the presence of bromine and ni

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the formation of complex heterocyclic compounds that are active in biological systems. Commonly employed in medicinal chemistry for constructing nitrogen-containing ring systems. Also utilized in agrochemical research for designing new bioactive molecules. Suitable for coupling reactions in organic synthesis due to the presence of bromine and nitrile functional groups.

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