tert-Butyl ((1-aminocyclohexyl)methyl)carbamate

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Reagent Code: #152798
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CAS Number 1352999-04-2

science Other reagents with same CAS 1352999-04-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.33 g/mol
Formula C₁₂H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD21091404
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for selective modification in active pharmaceutical ingredients, enhancing stability and bioavailability. Commonly employed in the preparation of cyclohexylamine derivatives with potential anxiolytic or analgesic properties. Also utilized in research settings for building complex nitrogen-containing molecules through selective amine protection and coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,900.00
inventory 250mg
10-20 days ฿3,290.00
inventory 1g
10-20 days ฿7,040.00
inventory 5g
10-20 days ฿24,540.00

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tert-Butyl ((1-aminocyclohexyl)methyl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for selective modification in active pharmaceutical ingredients, enhancing stability and bioavailability. Commonly employed in the preparation of cyclohexylamine derivatives with potential anxiolytic or analgesic properties. Also utilized in research settings for building complex nitrogen-containing molecules through selective amine p
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for selective modification in active pharmaceutical ingredients, enhancing stability and bioavailability. Commonly employed in the preparation of cyclohexylamine derivatives with potential anxiolytic or analgesic properties. Also utilized in research settings for building complex nitrogen-containing molecules through selective amine protection and coupling reactions.
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