(S)-tert-Butyl 2-(cyanomethyl)azetidine-1-carboxylate

95%

Reagent Code: #38177
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CAS Number 228868-28-8

science Other reagents with same CAS 228868-28-8

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Weight 196.2462 g/mol
Formula C₁₀H₁₆N₂O₂
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description Product Description

This chemical is primarily used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure, featuring an azetidine ring and a cyano group, makes it valuable for constructing complex organic compounds. It is often employed in medicinal chemistry to create inhibitors or modulators of biological targets, such as enzymes or receptors. Additionally, it can be utilized in peptide synthesis and the preparation of chiral compounds due to its stereocenter. Its tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes.

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inventory 50mg
10-20 days ฿8,020.00

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(S)-tert-Butyl 2-(cyanomethyl)azetidine-1-carboxylate
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This chemical is primarily used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure, featuring an azetidine ring and a cyano group, makes it valuable for constructing complex organic compounds. It is often employed in medicinal chemistry to create inhibitors or modulators of biological targets, such as enzymes or receptors. Additionally, it can be utilized in peptide synthesis and the preparation of chiral compo

This chemical is primarily used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure, featuring an azetidine ring and a cyano group, makes it valuable for constructing complex organic compounds. It is often employed in medicinal chemistry to create inhibitors or modulators of biological targets, such as enzymes or receptors. Additionally, it can be utilized in peptide synthesis and the preparation of chiral compounds due to its stereocenter. Its tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes.

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