(S)-Benzyl (1-cyanoethyl)carbamate

98%

Reagent Code: #232849
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CAS Number 17343-54-3

science Other reagents with same CAS 17343-54-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.23 g/mol
Formula C₁₁H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD03094748
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of optically active compounds such as protease inhibitors and other bioactive molecules. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where it helps control stereochemistry during drug development. Commonly employed in the preparation of β-amino acids and peptide mimetics due to the stability and reactivity of the cyano and carbamate functional groups. Also utilized in the construction of complex molecules in medicinal chemistry research, especially in routes requiring protection of amine functionalities with orthogonal deprotection options.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,120.00
inventory 250mg
10-20 days ฿6,900.00
inventory 1g
10-20 days ฿18,540.00
(S)-Benzyl (1-cyanoethyl)carbamate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of optically active compounds such as protease inhibitors and other bioactive molecules. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where it helps control stereochemistry during drug development. Commonly employed in the preparation of β-amino acids and peptide mimetics due to the stability and reactivity of the cyano and carbamate functional groups. Also utilized in the c

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of optically active compounds such as protease inhibitors and other bioactive molecules. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where it helps control stereochemistry during drug development. Commonly employed in the preparation of β-amino acids and peptide mimetics due to the stability and reactivity of the cyano and carbamate functional groups. Also utilized in the construction of complex molecules in medicinal chemistry research, especially in routes requiring protection of amine functionalities with orthogonal deprotection options.

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