1-Benzyl-3-carbamoylpyridin-1-ium bromide

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Reagent Code: #150395
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CAS Number 13076-43-2

science Other reagents with same CAS 13076-43-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.16 g/mol
Formula C₁₃H₁₃BrN₂O
badge Registry Numbers
MDL Number MFCD00160345
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a precursor in the synthesis of nicotinamide adenine dinucleotide (NAD) analogs, which are important in biochemical and pharmaceutical research. It serves as a building block in the development of enzyme cofactor mimics, particularly in redox reactions involving dehydrogenases. Its structural features make it suitable for studying electron transfer processes and designing inhibitors or activators in metabolic pathways. Also employed in the preparation of ionic liquids for catalytic applications due to its stable pyridinium core and solubility properties.

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Test Parameter Specification
Appearance white solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,980.00
inventory 250mg
10-20 days ฿7,500.00
inventory 1g
10-20 days ฿16,000.00

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1-Benzyl-3-carbamoylpyridin-1-ium bromide
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Used as a precursor in the synthesis of nicotinamide adenine dinucleotide (NAD) analogs, which are important in biochemical and pharmaceutical research. It serves as a building block in the development of enzyme cofactor mimics, particularly in redox reactions involving dehydrogenases. Its structural features make it suitable for studying electron transfer processes and designing inhibitors or activators in metabolic pathways. Also employed in the preparation of ionic liquids for catalytic applications d

Used as a precursor in the synthesis of nicotinamide adenine dinucleotide (NAD) analogs, which are important in biochemical and pharmaceutical research. It serves as a building block in the development of enzyme cofactor mimics, particularly in redox reactions involving dehydrogenases. Its structural features make it suitable for studying electron transfer processes and designing inhibitors or activators in metabolic pathways. Also employed in the preparation of ionic liquids for catalytic applications due to its stable pyridinium core and solubility properties.

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