tert-Butyl ((1S,3S)-3-aminocyclohexyl)carbamate

98%

Reagent Code: #233314
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CAS Number 1788036-28-1

science Other reagents with same CAS 1788036-28-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.3 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD18632893
thermostat Physical Properties
Boiling Point 322.1±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.02±0.1 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral cyclohexylamine scaffolds. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in the production of drugs targeting central nervous system disorders and metabolic diseases due to its structural stability and stereochemical purity. Also utilized in the preparation of protease inhibitors and other bioactive molecules where precise stereochemistry is critical for activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,430.00
inventory 250mg
10-20 days ฿32,120.00
tert-Butyl ((1S,3S)-3-aminocyclohexyl)carbamate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral cyclohexylamine scaffolds. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in the production of drugs targeting central nervous system disorders and metabolic diseases due to its structural stability and stereochemical purity. Also utilized in the preparation of protease inh

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral cyclohexylamine scaffolds. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in the production of drugs targeting central nervous system disorders and metabolic diseases due to its structural stability and stereochemical purity. Also utilized in the preparation of protease inhibitors and other bioactive molecules where precise stereochemistry is critical for activity.

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