2-Amino-6-bromo-3,5-difluorobenzoic acid

95%

Reagent Code: #137208
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CAS Number 1602151-62-1

science Other reagents with same CAS 1602151-62-1

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Weight 252.01 g/mol
Formula C₇H₄BrF₂NO₂
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Storage Room temperature

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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective substitution reactions, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in research settings to design drugs targeting cancer, inflammation, and central nervous system disorders. Also utilized in the preparation of agrochemicals and specialty organic materials due to its halogen and amino functional groups, which facilitate coupling reactions and molecular diversification.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,220.00
inventory 250mg
10-20 days ฿22,400.00
inventory 1g
10-20 days ฿56,320.00

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2-Amino-6-bromo-3,5-difluorobenzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective substitution reactions, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in research settings to design drugs targeting cancer, inflammation, and central nervous system disorders. Also utilized in the preparation of agrochemicals and specialty organic materials due to

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective substitution reactions, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in research settings to design drugs targeting cancer, inflammation, and central nervous system disorders. Also utilized in the preparation of agrochemicals and specialty organic materials due to its halogen and amino functional groups, which facilitate coupling reactions and molecular diversification.

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