(S)-2-((tert-butoxycarbonyl)amino)-2-(1-methylcyclohexyl)acetic acid

98%

Reagent Code: #237069
fingerprint
CAS Number 951789-86-9

science Other reagents with same CAS 951789-86-9

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its sterically hindered cyclohexyl group and protected amine functionality make it valuable for peptide mimetics and structure-activity relationship studies. Commonly employed in asymmetric synthesis to introduce stereochemical control. The Boc-protected amine allows for selective deprotection and coupling in multi-step organic syntheses, especially in drug discovery targeting central nervous system disorders and metabolic diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,460.00
inventory 100mg
10-20 days ฿16,070.00
inventory 250mg
10-20 days ฿26,490.00
inventory 1g
10-20 days ฿81,300.00
(S)-2-((tert-butoxycarbonyl)amino)-2-(1-methylcyclohexyl)acetic acid
No image available

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its sterically hindered cyclohexyl group and protected amine functionality make it valuable for peptide mimetics and structure-activity relationship studies. Commonly employed in asymmetric synthesis to introduce stereochemical control. The Boc-protected amine allows for selective deprotection and coupling in multi-step organic syntheses,

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its sterically hindered cyclohexyl group and protected amine functionality make it valuable for peptide mimetics and structure-activity relationship studies. Commonly employed in asymmetric synthesis to introduce stereochemical control. The Boc-protected amine allows for selective deprotection and coupling in multi-step organic syntheses, especially in drug discovery targeting central nervous system disorders and metabolic diseases.

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...