Ethyl 6-hydroxynicotinate

98%

Reagent Code: #182495
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CAS Number 18617-50-0

science Other reagents with same CAS 18617-50-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.16 g/mol
Formula C₈H₉NO₃
thermostat Physical Properties
Boiling Point 347.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives with potential antihypertensive and anti-inflammatory activity. Commonly employed in the development of NAD (nicotinamide adenine dinucleotide) analogs for biochemical research. Also serves as a building block in the preparation of heterocyclic compounds for drug discovery and in agrochemical formulations for crop protection agents. Its hydroxyl and ester functional groups allow for easy modification in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,900.00
inventory 100g
10-20 days ฿10,310.00

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Ethyl 6-hydroxynicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives with potential antihypertensive and anti-inflammatory activity. Commonly employed in the development of NAD (nicotinamide adenine dinucleotide) analogs for biochemical research. Also serves as a building block in the preparation of heterocyclic compounds for drug discovery and in agrochemical formulations for crop protection agents. Its hydroxyl and ester functional groups allow fo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acid derivatives with potential antihypertensive and anti-inflammatory activity. Commonly employed in the development of NAD (nicotinamide adenine dinucleotide) analogs for biochemical research. Also serves as a building block in the preparation of heterocyclic compounds for drug discovery and in agrochemical formulations for crop protection agents. Its hydroxyl and ester functional groups allow for easy modification in multi-step organic syntheses.

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