2-(Hydroxymethyl)isonicotinaldehyde

90%

Reagent Code: #196568
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CAS Number 1155873-00-9

science Other reagents with same CAS 1155873-00-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.14 g/mol
Formula C₇H₇NO₂
badge Registry Numbers
MDL Number MFCD18384274
thermostat Physical Properties
Boiling Point 300.0±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.268±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and vitamin B3 derivatives. It serves as a building block in the preparation of biologically active molecules, including enzyme inhibitors and receptor modulators. Its aldehyde and hydroxymethyl functional groups allow for versatile chemical modifications, making it valuable in medicinal chemistry for creating novel compounds with potential antimicrobial, anti-inflammatory, or neuroprotective properties. Also employed in the synthesis of fluorescent probes and sensors due to its ability to form conjugated systems upon condensation reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,900.00
inventory 250mg
10-20 days ฿11,840.00
inventory 1g
10-20 days ฿36,290.00

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2-(Hydroxymethyl)isonicotinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and vitamin B3 derivatives. It serves as a building block in the preparation of biologically active molecules, including enzyme inhibitors and receptor modulators. Its aldehyde and hydroxymethyl functional groups allow for versatile chemical modifications, making it valuable in medicinal chemistry for creating novel compounds with potential antimicrobial, anti-inflammatory, or neuro

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and vitamin B3 derivatives. It serves as a building block in the preparation of biologically active molecules, including enzyme inhibitors and receptor modulators. Its aldehyde and hydroxymethyl functional groups allow for versatile chemical modifications, making it valuable in medicinal chemistry for creating novel compounds with potential antimicrobial, anti-inflammatory, or neuroprotective properties. Also employed in the synthesis of fluorescent probes and sensors due to its ability to form conjugated systems upon condensation reactions.

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