6-Chloro-4-methylnicotinamide

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Reagent Code: #163543
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CAS Number 65169-37-1

science Other reagents with same CAS 65169-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.60 g/mol
Formula C₇H₇ClN₂O
badge Registry Numbers
MDL Number MFCD20704788
thermostat Physical Properties
Melting Point 166-167 °C
Boiling Point 303.5±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.316±0.06 g/cm3(Predicted)
Storage Room temperature, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs targeting metabolic and neurological disorders. It serves in the preparation of bioactive molecules due to its structural similarity to vitamin B3 derivatives, enabling modulation of enzyme activity in cellular processes. Commonly employed in research settings for designing compounds with potential antidiabetic, anti-inflammatory, or neuroprotective properties. Its chloro and methyl functional groups allow for selective chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,550.00
inventory 250mg
10-20 days ฿8,450.00
inventory 1g
10-20 days ฿16,900.00

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6-Chloro-4-methylnicotinamide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs targeting metabolic and neurological disorders. It serves in the preparation of bioactive molecules due to its structural similarity to vitamin B3 derivatives, enabling modulation of enzyme activity in cellular processes. Commonly employed in research settings for designing compounds with potential antidiabetic, anti-inflammatory, or neuroprotective properties. Its chloro and methyl

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs targeting metabolic and neurological disorders. It serves in the preparation of bioactive molecules due to its structural similarity to vitamin B3 derivatives, enabling modulation of enzyme activity in cellular processes. Commonly employed in research settings for designing compounds with potential antidiabetic, anti-inflammatory, or neuroprotective properties. Its chloro and methyl functional groups allow for selective chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

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