tert-Butyl 6-aminopicolinate

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Reagent Code: #49673
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CAS Number 1499890-31-1

science Other reagents with same CAS 1499890-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.2304 g/mol
Formula C₁₀H₁₄N₂O₂
badge Registry Numbers
MDL Number MFCD24127898
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description Product Description

Tert-Butyl 6-aminopicolinate is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as anti-inflammatory, anticancer, and antiviral agents. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules through reactions like amidation, esterification, and coupling processes. Its role in medicinal chemistry is significant, as it contributes to the design and optimization of drug candidates with improved efficacy and safety profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,330.00
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tert-Butyl 6-aminopicolinate
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Tert-Butyl 6-aminopicolinate is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as anti-inflammatory, anticancer, and antiviral agents. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules through reactions like amidation, esterification, and coupling pr

Tert-Butyl 6-aminopicolinate is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as anti-inflammatory, anticancer, and antiviral agents. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules through reactions like amidation, esterification, and coupling processes. Its role in medicinal chemistry is significant, as it contributes to the design and optimization of drug candidates with improved efficacy and safety profiles.

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