3-(Hydroxymethyl)benzamide

95%

Reagent Code: #196449
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CAS Number 126926-34-9

science Other reagents with same CAS 126926-34-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.16 g/mol
Formula C₈H₉NO₂
badge Registry Numbers
MDL Number MFCD12137892
thermostat Physical Properties
Boiling Point 338.8 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.239 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its functional groups—hydroxyl and amide—allow for derivatization in drug development, particularly in the preparation of benzamide-based molecules with potential neurological or anti-inflammatory activity. Also employed in the design of enzyme inhibitors due to its ability to interact with active sites through hydrogen bonding. Serves as a building block in medicinal chemistry for creating libraries of compounds for screening.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,060.00
inventory 250mg
10-20 days ฿11,470.00
inventory 1g
10-20 days ฿34,380.00

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3-(Hydroxymethyl)benzamide
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its functional groups—hydroxyl and amide—allow for derivatization in drug development, particularly in the preparation of benzamide-based molecules with potential neurological or anti-inflammatory activity. Also employed in the design of enzyme inhibitors due to its ability to interact with active sites through hydrogen bonding. Serves as a building block in medicinal chemistry for creating libraries of compounds for s
Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its functional groups—hydroxyl and amide—allow for derivatization in drug development, particularly in the preparation of benzamide-based molecules with potential neurological or anti-inflammatory activity. Also employed in the design of enzyme inhibitors due to its ability to interact with active sites through hydrogen bonding. Serves as a building block in medicinal chemistry for creating libraries of compounds for screening.
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