[3,4'-Bipyridine]-1'(2'H)-carboxylic acid, 2-chloro-3',6'-dihydro-, 1,1-dimethylethyl ester

95%

Reagent Code: #142271
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CAS Number 1621910-17-5

science Other reagents with same CAS 1621910-17-5

blur_circular Chemical Specifications

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Weight 294.78 g/mol
Formula C₁₅H₁₉ClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where nitrogen-containing scaffolds are required for optimal binding to enzymes or receptors. Its protected ester form allows for selective deprotection and further functionalization in multi-step synthesis.

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inventory 1g
10-20 days ฿28,500.00

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[3,4'-Bipyridine]-1'(2'H)-carboxylic acid, 2-chloro-3',6'-dihydro-, 1,1-dimethylethyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where nitrogen-containing scaffolds are required for optimal binding to enzymes or receptors. Its protected ester form allows for sel

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where nitrogen-containing scaffolds are required for optimal binding to enzymes or receptors. Its protected ester form allows for selective deprotection and further functionalization in multi-step synthesis.

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