Tetrahydropyran-2-carboxylic Acid

≥95%

Reagent Code: #172531
fingerprint
CAS Number 51673-83-7

science Other reagents with same CAS 51673-83-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.14 g/mol
Formula C₆H₁₀O₃
badge Registry Numbers
MDL Number MFCD07779239
inventory_2 Storage & Handling
Storage Room temperature, 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 rigid cyclic structure helps influence the conformation of peptide-like compounds, enhancing metabolic stability and binding selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic natural amino acids while providing improved pharmacokinetic properties. Also utilized in the preparation of organocatalysts and as an intermediate in asymmetric synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿510.00
inventory 5g
10-20 days ฿1,720.00
inventory 10g
10-20 days ฿3,400.00
inventory 25g
10-20 days ฿8,450.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Tetrahydropyran-2-carboxylic Acid
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 rigid cyclic structure helps influence the conformation of peptide-like compounds, enhancing metabolic stability and binding selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic natural amino acids while providing improved pharmacokinetic properties. Also utilized in the

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its rigid cyclic structure helps influence the conformation of peptide-like compounds, enhancing metabolic stability and binding selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic natural amino acids while providing improved pharmacokinetic properties. Also utilized in the preparation of organocatalysts and as an intermediate in asymmetric synthesis.

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...