rel-Methyl (1R,3S)-3-((tert-butoxycarbonyl)amino)-1-methylcyclohexane-1-carboxylate

98%

Reagent Code: #229328
fingerprint
CAS Number 2828439-35-4

science Other reagents with same CAS 2828439-35-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.35 g/mol
Formula C₁₄H₂₅NO₄
thermostat Physical Properties
Boiling Point 353.3±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.05±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and ester functional groups allow for selective transformations in multi-step organic syntheses. The stereochemistry of the compound makes it valuable for creating enantiomerically pure drugs, especially in research targeting central nervous system agents and antiviral compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and defined stereochemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,430.00
inventory 250mg
10-20 days ฿29,610.00
inventory 1g
10-20 days ฿79,860.00
rel-Methyl (1R,3S)-3-((tert-butoxycarbonyl)amino)-1-methylcyclohexane-1-carboxylate
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and ester functional groups allow for selective transformations in multi-step organic syntheses. The stereochemistry of the compound makes it valuable for creating enantiomerically pure drugs, especially in research targeting central nervous system agents and antiviral compounds. Commonly employed in medicinal chemistry for structur

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and ester functional groups allow for selective transformations in multi-step organic syntheses. The stereochemistry of the compound makes it valuable for creating enantiomerically pure drugs, especially in research targeting central nervous system agents and antiviral compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and defined stereochemistry.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...