2-Bromo-3,5-dimethylpyrazine

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Reagent Code: #148122
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CAS Number 91678-74-9

science Other reagents with same CAS 91678-74-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.04 g/mol
Formula C₆H₇BrN₂
badge Registry Numbers
MDL Number MFCD18250493
inventory_2 Storage & Handling
Storage 2-8℃, inert gas

description Product Description

Used primarily as a flavor and fragrance ingredient due to its potent aroma. It contributes roasted, nutty, and meaty notes, making it valuable in the food industry for enhancing savory flavors, especially in processed foods, soups, and seasonings. Also employed in the synthesis of more complex organic molecules, particularly in pharmaceutical and agrochemical research, where it serves as a building block for introducing pyrazine rings. Its bromine functionality allows for further chemical modifications through cross-coupling reactions, enabling the development of specialized intermediates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,400.00
inventory 1g
10-20 days ฿18,620.00

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2-Bromo-3,5-dimethylpyrazine
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Used primarily as a flavor and fragrance ingredient due to its potent aroma. It contributes roasted, nutty, and meaty notes, making it valuable in the food industry for enhancing savory flavors, especially in processed foods, soups, and seasonings. Also employed in the synthesis of more complex organic molecules, particularly in pharmaceutical and agrochemical research, where it serves as a building block for introducing pyrazine rings. Its bromine functionality allows for further chemical modifications

Used primarily as a flavor and fragrance ingredient due to its potent aroma. It contributes roasted, nutty, and meaty notes, making it valuable in the food industry for enhancing savory flavors, especially in processed foods, soups, and seasonings. Also employed in the synthesis of more complex organic molecules, particularly in pharmaceutical and agrochemical research, where it serves as a building block for introducing pyrazine rings. Its bromine functionality allows for further chemical modifications through cross-coupling reactions, enabling the development of specialized intermediates.

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