ethyl 3-(cyclohexylamino)-2-hydroxy-2-methylpropanoate

Reagent Code: #181204
fingerprint
CAS Number 1137869-65-8

science Other reagents with same CAS 1137869-65-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.32 g/mol
Formula C₁₂H₂₃NO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its structure allows for functionalization in multi-step reactions, making it valuable in creating complex molecules with potential therapeutic properties. Commonly employed in the preparation of beta-blocker analogs and other cardiovascular agents due to the presence of amino and hydroxy groups that mimic pharmacophores in adrenergic blockers. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies, where the cyclohexylamino moiety contributes to lipophilicity and membrane permeability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,900.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
ethyl 3-(cyclohexylamino)-2-hydroxy-2-methylpropanoate
No image available

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its structure allows for functionalization in multi-step reactions, making it valuable in creating complex molecules with potential therapeutic properties. Commonly employed in the preparation of beta-blocker analogs and other cardiovascular agents due to the presence of amino and hydroxy groups that mimic pharmacophores in adrenergic blockers. Also utilized in medicinal chemistry res

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its structure allows for functionalization in multi-step reactions, making it valuable in creating complex molecules with potential therapeutic properties. Commonly employed in the preparation of beta-blocker analogs and other cardiovascular agents due to the presence of amino and hydroxy groups that mimic pharmacophores in adrenergic blockers. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies, where the cyclohexylamino moiety contributes to lipophilicity and membrane permeability.

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...