(9H-Fluoren-9-yl)methyl (trans-4-aminocyclohexyl)carbamate hydrochloride

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Reagent Code: #37155
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CAS Number 672310-17-7

science Other reagents with same CAS 672310-17-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.8900 g/mol
Formula C₂₁H₂₄N₂O₂HCl
badge Registry Numbers
MDL Number MFCD03001746
inventory_2 Storage & Handling
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description Product Description

This Fmoc-protected trans-4-aminocyclohexylamine hydrochloride is primarily used as a building block in the field of peptide synthesis. The (9H-fluoren-9-yl)methyl (Fmoc) group protects one of the amine functions, providing stability under basic conditions and facile removal under mild acidic conditions in solid-phase peptide synthesis (SPPS). The free amine (as hydrochloride salt) enables selective coupling reactions. The trans-4-aminocyclohexyl moiety enhances the solubility and handling properties of the compound, making it suitable for automated peptide synthesizers. It is widely applied in the production of pharmaceuticals, bioactive peptides, and research reagents, ensuring high purity and yield in the synthesis process. Additionally, its hydrochloride salt form improves stability and shelf life, making it convenient for storage and use in laboratory settings.

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Test Parameter Specification
Appearance White Powder
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,304.00

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(9H-Fluoren-9-yl)methyl (trans-4-aminocyclohexyl)carbamate hydrochloride
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This Fmoc-protected trans-4-aminocyclohexylamine hydrochloride is primarily used as a building block in the field of peptide synthesis. The (9H-fluoren-9-yl)methyl (Fmoc) group protects one of the amine functions, providing stability under basic conditions and facile removal under mild acidic conditions in solid-phase peptide synthesis (SPPS). The free amine (as hydrochloride salt) enables selective coupling reactions. The trans-4-aminocyclohexyl moiety enhances the solubility and handling properties of

This Fmoc-protected trans-4-aminocyclohexylamine hydrochloride is primarily used as a building block in the field of peptide synthesis. The (9H-fluoren-9-yl)methyl (Fmoc) group protects one of the amine functions, providing stability under basic conditions and facile removal under mild acidic conditions in solid-phase peptide synthesis (SPPS). The free amine (as hydrochloride salt) enables selective coupling reactions. The trans-4-aminocyclohexyl moiety enhances the solubility and handling properties of the compound, making it suitable for automated peptide synthesizers. It is widely applied in the production of pharmaceuticals, bioactive peptides, and research reagents, ensuring high purity and yield in the synthesis process. Additionally, its hydrochloride salt form improves stability and shelf life, making it convenient for storage and use in laboratory settings.

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