2-Amino-6-chloropyridin-3-ol

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Reagent Code: #137900
label
Alias 2-amino-6-chloro-3-hydroxypyridine
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CAS Number 159309-66-7

science Other reagents with same CAS 159309-66-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.56 g/mol
Formula C₅H₅ClN₂O
badge Registry Numbers
MDL Number MFCD13189893
inventory_2 Storage & Handling
Storage 2-8°C, inert gas, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive and anti-inflammatory drugs. It serves as a building block in the development of kinase inhibitors and other biologically active compounds due to its ability to form hydrogen bonds and participate in aromatic interactions. Also applied in agrochemical synthesis for creating herbicides and pesticides with improved selectivity. Its structural features, including the amino, hydroxy, and chloro substituents on the pyridine ring, make it valuable in medicinal chemistry for optimizing drug potency and metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,018.50
inventory 250mg
10-20 days ฿3,234.00
inventory 1g
10-20 days ฿8,415.00

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2-Amino-6-chloropyridin-3-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive and anti-inflammatory drugs. It serves as a building block in the development of kinase inhibitors and other biologically active compounds due to its ability to form hydrogen bonds and participate in aromatic interactions. Also applied in agrochemical synthesis for creating herbicides and pesticides with improved selectivity. Its structural features, including the amino, hydroxy, and chloro

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive and anti-inflammatory drugs. It serves as a building block in the development of kinase inhibitors and other biologically active compounds due to its ability to form hydrogen bonds and participate in aromatic interactions. Also applied in agrochemical synthesis for creating herbicides and pesticides with improved selectivity. Its structural features, including the amino, hydroxy, and chloro substituents on the pyridine ring, make it valuable in medicinal chemistry for optimizing drug potency and metabolic stability.

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