(1S,3R)-5-Bromo-3-Hydroxy-2,3-Dihydrospiro[Indene-1,5’-Oxazolidine]-2’,4’-Dione

98%

Reagent Code: #237357
fingerprint
CAS Number 1889291-47-7

science Other reagents with same CAS 1889291-47-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.09 g/mol
Formula C₁₁H₈BrNO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules. Its spirocyclic structure and stereochemistry make it valuable in developing enantioselective catalysts and novel drug candidates, particularly in central nervous system agents and anti-inflammatory compounds. The bromo and hydroxy functional groups allow for further chemical modifications, enabling structure-activity relationship studies. Also employed in the preparation of specialty heterocyclic compounds for use in asymmetric synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿41,180.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(1S,3R)-5-Bromo-3-Hydroxy-2,3-Dihydrospiro[Indene-1,5’-Oxazolidine]-2’,4’-Dione
No image available

Used in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules. Its spirocyclic structure and stereochemistry make it valuable in developing enantioselective catalysts and novel drug candidates, particularly in central nervous system agents and anti-inflammatory compounds. The bromo and hydroxy functional groups allow for further chemical modifications, enabling structure-activity relationship studies. Also employed in the preparation of specialty heterocyclic compounds for

Used in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules. Its spirocyclic structure and stereochemistry make it valuable in developing enantioselective catalysts and novel drug candidates, particularly in central nervous system agents and anti-inflammatory compounds. The bromo and hydroxy functional groups allow for further chemical modifications, enabling structure-activity relationship studies. Also employed in the preparation of specialty heterocyclic compounds for use in asymmetric synthesis.

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...