(-)-2,2'-Isopropylidenebis[(4S)-4-phenyl-2-oxazoline]

97%

Reagent Code: #126677
label
Alias (S,S)-2,2'-Isopropylidene bis(4-phenyl-2-oxazoline)
fingerprint
CAS Number 131457-46-0

science Other reagents with same CAS 131457-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.41 g/mol
Formula C₂₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD00192245
thermostat Physical Properties
Melting Point 37-41 °C(lit.)
Boiling Point 193 °C0.03 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1 g/mL at 25 °C(lit.)
Storage -20°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as asymmetric hydrogenation, to produce optically active compounds with high enantiomeric purity. Its application extends to the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the control of stereochemistry is essential for efficacy and safety. Additionally, it can be used in the preparation of chiral catalysts and as a building block for more complex chiral frameworks in organic synthesis.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to yellow viscous liquid or solid
Purity (%) 97
Specific Rotation [A]20/D (C=1 in Ethanol) -173 to -151
Note This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,200.00
inventory 1g
10-20 days ฿9,850.00
inventory 5g
10-20 days ฿27,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(-)-2,2'-Isopropylidenebis[(4S)-4-phenyl-2-oxazoline]
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as asymmetric hydrogenation, to produce optically active compounds with high enantiomeric purity. Its application extends to the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the control of stereochemistry is essential for efficacy and safety. Additionally, it can

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as asymmetric hydrogenation, to produce optically active compounds with high enantiomeric purity. Its application extends to the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the control of stereochemistry is essential for efficacy and safety. Additionally, it can be used in the preparation of chiral catalysts and as a building block for more complex chiral frameworks in organic 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...