(S)-2-Methoxypropan-1-amine

98%

Reagent Code: #237054
fingerprint
CAS Number 907943-71-9

science Other reagents with same CAS 907943-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 89.14 g/mol
Formula C₄H₁₁NO
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients where stereochemistry plays a critical role in biological activity. Its amine and methoxy functional groups allow for versatile reactivity, making it valuable in asymmetric synthesis. Commonly employed in the preparation of beta-blockers and other cardiovascular drugs, as well as in agrochemicals requiring enantiomerically pure intermediates. Also utilized in the manufacture of specialty polymers and catalysts where chirality influences performance.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,350.00
inventory 250mg
10-20 days ฿5,360.00
inventory 1g
10-20 days ฿15,080.00
inventory 5g
10-20 days ฿61,600.00
(S)-2-Methoxypropan-1-amine
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients where stereochemistry plays a critical role in biological activity. Its amine and methoxy functional groups allow for versatile reactivity, making it valuable in asymmetric synthesis. Commonly employed in the preparation of beta-blockers and other cardiovascular drugs, as well as in agrochemicals requiring enantiomerically pure intermediates. Also utilized in the manufacture of speci

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients where stereochemistry plays a critical role in biological activity. Its amine and methoxy functional groups allow for versatile reactivity, making it valuable in asymmetric synthesis. Commonly employed in the preparation of beta-blockers and other cardiovascular drugs, as well as in agrochemicals requiring enantiomerically pure intermediates. Also utilized in the manufacture of specialty polymers and catalysts where chirality influences performance.

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...