2-Amino-5-bromo-3-methylbenzonitrile

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Reagent Code: #116323
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CAS Number 1093966-37-0

science Other reagents with same CAS 1093966-37-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.06 g/mol
Formula C₈H₇BrN₂
badge Registry Numbers
MDL Number MFCD22024490
inventory_2 Storage & Handling
Storage Room temperature, dark, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of compounds with potential biological activity, particularly in the development of drugs targeting central nervous system disorders. Its bromo and nitrile groups make it a versatile building block for constructing complex molecules through various chemical reactions, such as cross-coupling and cyclization. Additionally, it is employed in research settings for the development of novel organic materials and dyes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,535.00
inventory 100mg
10-20 days ฿3,690.00
inventory 1g
10-20 days ฿13,833.00

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2-Amino-5-bromo-3-methylbenzonitrile
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of compounds with potential biological activity, particularly in the development of drugs targeting central nervous system disorders. Its bromo and nitrile groups make it a versatile building block for constructing complex molecules through various chemical reactions, such as cross-coupling and cyclization. Additionally, it is employed in research settings for the development of

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of compounds with potential biological activity, particularly in the development of drugs targeting central nervous system disorders. Its bromo and nitrile groups make it a versatile building block for constructing complex molecules through various chemical reactions, such as cross-coupling and cyclization. Additionally, it is employed in research settings for the development of novel organic materials and dyes.

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