3-(Bromomethyl)benzamide

95%

Reagent Code: #146047
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CAS Number 509073-67-0

science Other reagents with same CAS 509073-67-0

blur_circular Chemical Specifications

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Weight 214.06 g/mol
Formula C₈H₈BrNO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and biologically active molecules. The bromomethyl group allows for easy alkylation or substitution reactions, making it valuable in the construction of more complex structures. It is often employed in the development of drug candidates targeting central nervous system disorders and inflammatory conditions. Additionally, its amide functionality enables hydrogen bonding, which can enhance binding affinity in medicinal chemistry applications. It is also utilized in the synthesis of agrochemicals and functional materials where controlled reactivity is required.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,200.00
inventory 250mg
10-20 days ฿4,180.00
inventory 1g
10-20 days ฿9,720.00

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3-(Bromomethyl)benzamide
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and biologically active molecules. The bromomethyl group allows for easy alkylation or substitution reactions, making it valuable in the construction of more complex structures. It is often employed in the development of drug candidates targeting central nervous system disorders and inflammatory conditions. Additionally, its amide functionality enables hydrogen bonding, which can e

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and biologically active molecules. The bromomethyl group allows for easy alkylation or substitution reactions, making it valuable in the construction of more complex structures. It is often employed in the development of drug candidates targeting central nervous system disorders and inflammatory conditions. Additionally, its amide functionality enables hydrogen bonding, which can enhance binding affinity in medicinal chemistry applications. It is also utilized in the synthesis of agrochemicals and functional materials where controlled reactivity is required.

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