Methyl 6-(aminomethyl)picolinate hydrochloride

≥95%

Reagent Code: #209145
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CAS Number 171670-23-8

science Other reagents with same CAS 171670-23-8

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scatter_plot Molecular Information
Weight 202.64 g/mol
Formula C₈H₁₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD16660686
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in research settings to prepare analogs for drug discovery programs, especially in oncology and inflammation-related therapies. Also utilized in the preparation of peptide mimetics and as a building block in combinatorial chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,270.00
inventory 250mg
10-20 days ฿2,490.00
inventory 1g
10-20 days ฿5,240.00
inventory 10g
10-20 days ฿42,890.00
inventory 5g
10-20 days ฿24,650.00

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Methyl 6-(aminomethyl)picolinate hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in research settings to prepare analogs for drug discovery programs, especially in oncology and inflammation-related therapies. Also utilized in the preparation of peptide mimetics and as a building block in

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in research settings to prepare analogs for drug discovery programs, especially in oncology and inflammation-related therapies. Also utilized in the preparation of peptide mimetics and as a building block in combinatorial chemistry.

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