(2-amino-6-chloropyridin-4-yl)methanol

≥95%

Reagent Code: #139484
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CAS Number 1334294-36-8

science Other reagents with same CAS 1334294-36-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.59 g/mol
Formula C₆H₇ClN₂O
badge Registry Numbers
MDL Number MFCD24386928
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anti-inflammatory, antiviral, or anticancer activity. Commonly employed in research settings to build more complex heterocyclic systems. Also utilized in the preparation of agrochemicals and specialty chemicals where chloro- and amino-substituted pyridine derivatives are needed.

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inventory 1g
10-20 days ฿52,870.00

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(2-amino-6-chloropyridin-4-yl)methanol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anti-inflammatory, antiviral, or anticancer activity. Commonly employed in research settings to build more complex heterocyclic systems. Also utilized in the preparation of agrochemicals and specialty chemicals where chloro- and a

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anti-inflammatory, antiviral, or anticancer activity. Commonly employed in research settings to build more complex heterocyclic systems. Also utilized in the preparation of agrochemicals and specialty chemicals where chloro- and amino-substituted pyridine derivatives are needed.

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