(S)-()-1-Cyclohexylethylisocyanate

99%

Reagent Code: #232824
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CAS Number 93470-27-0

science Other reagents with same CAS 93470-27-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.22 g/mol
Formula C₉H₁₅NO
badge Registry Numbers
MDL Number MFCD05664074
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily in the synthesis of chiral pharmaceuticals and fine chemicals, this compound serves as a key intermediate in asymmetric synthesis. Its isocyanate group readily reacts with amines and alcohols, enabling the construction of ureas and carbamates with defined stereochemistry. It is especially valuable in the development of enantiomerically pure drugs, where the (S)-configuration plays a critical role in biological activity. The cyclohexylethyl moiety provides steric bulk and lipophilicity, which can enhance selectivity and stability in final active ingredients. Commonly employed in research and process chemistry for targeted molecule design.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿38,000.00
(S)-()-1-Cyclohexylethylisocyanate
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Used primarily in the synthesis of chiral pharmaceuticals and fine chemicals, this compound serves as a key intermediate in asymmetric synthesis. Its isocyanate group readily reacts with amines and alcohols, enabling the construction of ureas and carbamates with defined stereochemistry. It is especially valuable in the development of enantiomerically pure drugs, where the (S)-configuration plays a critical role in biological activity. The cyclohexylethyl moiety provides steric bulk and lipophilicity, which
Used primarily in the synthesis of chiral pharmaceuticals and fine chemicals, this compound serves as a key intermediate in asymmetric synthesis. Its isocyanate group readily reacts with amines and alcohols, enabling the construction of ureas and carbamates with defined stereochemistry. It is especially valuable in the development of enantiomerically pure drugs, where the (S)-configuration plays a critical role in biological activity. The cyclohexylethyl moiety provides steric bulk and lipophilicity, which can enhance selectivity and stability in final active ingredients. Commonly employed in research and process chemistry for targeted molecule design.
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