Tert-butyl methyl azetidine-1,3-dicarboxylate

≥95%

Reagent Code: #240199
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CAS Number 610791-05-4

science Other reagents with same CAS 610791-05-4

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Weight 215.25 g/mol
Formula C₁₀H₁₇NO₄
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MDL Number MFCD06656775
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its protected azetidine ring provides structural stability and enables selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the ring’s favorable metabolic and conformational properties. Also utilized in research settings for scaffold diversification in high-throughput screening libraries.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿750.00
inventory 10g
10-20 days ฿1,350.00
inventory 25g
10-20 days ฿3,200.00
inventory 100g
10-20 days ฿12,000.00

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Tert-butyl methyl azetidine-1,3-dicarboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its protected azetidine ring provides structural stability and enables selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the ring’s favorable metabolic and conformational properties. Also utilized in research sett
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its protected azetidine ring provides structural stability and enables selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the ring’s favorable metabolic and conformational properties. Also utilized in research settings for scaffold diversification in high-throughput screening libraries.
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