(R)-2-(Aminomethyl)-3-methylbutanoic acid

97%

Reagent Code: #230134
fingerprint
CAS Number 210345-86-1

science Other reagents with same CAS 210345-86-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 131.17 g/mol
Formula C₆H₁₃NO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antidiabetic agents. It serves as an intermediate in the production of DPP-4 inhibitors, which are used to manage type 2 diabetes by enhancing insulin release and reducing glucagon levels. Its stereochemistry is critical for biological activity, making it valuable in asymmetric synthesis. Also employed in the preparation of peptidomimetics and enzyme inhibitors due to its structural similarity to natural amino acids.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿181.50
inventory 100mg
10-20 days ฿940.00
inventory 500mg
10-20 days ฿1,947.00
inventory 5g
10-20 days ฿28,080.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-2-(Aminomethyl)-3-methylbutanoic acid
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antidiabetic agents. It serves as an intermediate in the production of DPP-4 inhibitors, which are used to manage type 2 diabetes by enhancing insulin release and reducing glucagon levels. Its stereochemistry is critical for biological activity, making it valuable in asymmetric synthesis. Also employed in the preparation of peptidomimetics and enzyme inhibitors due to its structural similarity to natur

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antidiabetic agents. It serves as an intermediate in the production of DPP-4 inhibitors, which are used to manage type 2 diabetes by enhancing insulin release and reducing glucagon levels. Its stereochemistry is critical for biological activity, making it valuable in asymmetric synthesis. Also employed in the preparation of peptidomimetics and enzyme inhibitors due to its structural similarity to natural amino acids.

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...