(8α,9S)-6'-Methoxycinchonan-9-amine trihydrochloride

97%

Reagent Code: #235721
fingerprint
CAS Number 1231763-32-8

science Other reagents with same CAS 1231763-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 432.82 g/mol
Formula C₁₀H₁₁ClO₂
badge Registry Numbers
MDL Number MFCD16875656
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily as a chiral catalyst or chiral auxiliary in asymmetric synthesis, enabling the production of enantiomerically enriched compounds. Its structure supports stereoselective transformations, particularly in hydrogenation and related reduction reactions. Widely applied in pharmaceutical manufacturing where precise stereochemistry is critical for drug efficacy and safety. Also employed in research settings for developing enantioselective methodologies in organic chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿790.00
inventory 250mg
10-20 days ฿2,900.00
inventory 1g
10-20 days ฿9,620.00
inventory 5g
10-20 days ฿25,560.00
(8α,9S)-6'-Methoxycinchonan-9-amine trihydrochloride
No image available

Used primarily as a chiral catalyst or chiral auxiliary in asymmetric synthesis, enabling the production of enantiomerically enriched compounds. Its structure supports stereoselective transformations, particularly in hydrogenation and related reduction reactions. Widely applied in pharmaceutical manufacturing where precise stereochemistry is critical for drug efficacy and safety. Also employed in research settings for developing enantioselective methodologies in organic chemistry.

Used primarily as a chiral catalyst or chiral auxiliary in asymmetric synthesis, enabling the production of enantiomerically enriched compounds. Its structure supports stereoselective transformations, particularly in hydrogenation and related reduction reactions. Widely applied in pharmaceutical manufacturing where precise stereochemistry is critical for drug efficacy and safety. Also employed in research settings for developing enantioselective methodologies in organic chemistry.

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...