2,5-Dichloro-4,6-dimethylnicotinamide

95%

Reagent Code: #130186
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CAS Number 175204-44-1

science Other reagents with same CAS 175204-44-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.07 g/mol
Formula C₈H₈Cl₂N₂O
badge Registry Numbers
MDL Number MFCD00052635
thermostat Physical Properties
Melting Point 172 °C
Boiling Point 255.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.388±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs with potential metabolic and neurological activity. It serves as a building block in agrochemicals for creating herbicides and plant growth regulators due to its stable heterocyclic structure. Also employed in research for designing enzyme inhibitors, especially those targeting NAD-dependent enzymes. Its chloro and methyl substitutions allow for selective functionalization in multi-step organic reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,920.00
inventory 1g
10-20 days ฿15,930.00
inventory 100mg
10-20 days ฿3,550.00

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2,5-Dichloro-4,6-dimethylnicotinamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs with potential metabolic and neurological activity. It serves as a building block in agrochemicals for creating herbicides and plant growth regulators due to its stable heterocyclic structure. Also employed in research for designing enzyme inhibitors, especially those targeting NAD-dependent enzymes. Its chloro and methyl substitutions allow for selective functionalization in multi-ste

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs with potential metabolic and neurological activity. It serves as a building block in agrochemicals for creating herbicides and plant growth regulators due to its stable heterocyclic structure. Also employed in research for designing enzyme inhibitors, especially those targeting NAD-dependent enzymes. Its chloro and methyl substitutions allow for selective functionalization in multi-step organic reactions.

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