(3R, 5S)-rel-3, 5-Dimethylmorpholine hydrochloride

98%

Reagent Code: #231109
fingerprint
CAS Number 154596-17-5

science Other reagents with same CAS 154596-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.63 g/mol
Formula C₆H₁₄ClNO
badge Registry Numbers
MDL Number MFCD14525805
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral auxiliary and enantioselective catalyst in organic synthesis, particularly in asymmetric reactions such as aldol condensations and alkylations. Its rigid morpholine ring and defined stereochemistry make it valuable for controlling stereochemical outcomes in pharmaceutical intermediates. Commonly employed in the development of active pharmaceutical ingredients (APIs) where precise stereochemistry is critical for biological activity. Also utilized in the preparation of protease inhibitors and other bioactive molecules requiring high enantiomeric purity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,170.00
inventory 250mg
10-20 days ฿1,940.00
inventory 1g
10-20 days ฿6,740.00
inventory 5g
10-20 days ฿29,250.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3R, 5S)-rel-3, 5-Dimethylmorpholine hydrochloride
No image available
Used as a chiral auxiliary and enantioselective catalyst in organic synthesis, particularly in asymmetric reactions such as aldol condensations and alkylations. Its rigid morpholine ring and defined stereochemistry make it valuable for controlling stereochemical outcomes in pharmaceutical intermediates. Commonly employed in the development of active pharmaceutical ingredients (APIs) where precise stereochemistry is critical for biological activity. Also utilized in the preparation of protease inhibitors and
Used as a chiral auxiliary and enantioselective catalyst in organic synthesis, particularly in asymmetric reactions such as aldol condensations and alkylations. Its rigid morpholine ring and defined stereochemistry make it valuable for controlling stereochemical outcomes in pharmaceutical intermediates. Commonly employed in the development of active pharmaceutical ingredients (APIs) where precise stereochemistry is critical for biological activity. Also utilized in the preparation of protease inhibitors and other bioactive molecules requiring high enantiomeric purity.
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...