(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2,3-dimethylbutanoicacid

>97%

Reagent Code: #235134
fingerprint
CAS Number 169566-81-8

science Other reagents with same CAS 169566-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 353.41 g/mol
Formula C₂₁H₂₃NO₄
thermostat Physical Properties
Boiling Point 554.1±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.209±0.06 g/cm3(Predicted)
Storage 2-8 °C

description Product Description

Used primarily in peptide synthesis as a chiral building block, this compound enables the introduction of a sterically hindered, branched-chain amino acid derivative with defined stereochemistry. Its Fmoc protection allows for solid-phase peptide synthesis under mild basic conditions, making it valuable for constructing complex peptides with enhanced metabolic stability and specific conformational properties. Commonly applied in the development of pharmaceuticals, bioactive peptides, and peptidomimetics where control over secondary structure and resistance to enzymatic degradation is critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,920.00
inventory 250mg
10-20 days ฿4,760.00
inventory 1g
10-20 days ฿18,950.00
inventory 5g
10-20 days ฿82,350.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2,3-dimethylbutanoicacid
No image available

Used primarily in peptide synthesis as a chiral building block, this compound enables the introduction of a sterically hindered, branched-chain amino acid derivative with defined stereochemistry. Its Fmoc protection allows for solid-phase peptide synthesis under mild basic conditions, making it valuable for constructing complex peptides with enhanced metabolic stability and specific conformational properties. Commonly applied in the development of pharmaceuticals, bioactive peptides, and peptidomimetics

Used primarily in peptide synthesis as a chiral building block, this compound enables the introduction of a sterically hindered, branched-chain amino acid derivative with defined stereochemistry. Its Fmoc protection allows for solid-phase peptide synthesis under mild basic conditions, making it valuable for constructing complex peptides with enhanced metabolic stability and specific conformational properties. Commonly applied in the development of pharmaceuticals, bioactive peptides, and peptidomimetics where control over secondary structure and resistance to enzymatic degradation is critical.

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...