(R,R)-()-2,2'-Isopropylidenebis(4-tert-butyl-2-oxazoline)

97%

Reagent Code: #69730
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CAS Number 131833-97-1

science Other reagents with same CAS 131833-97-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.44 g/mol
Formula C₁₇H₃₀N₂O₂
badge Registry Numbers
MDL Number MFCD07368371
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application extends to metal-catalyzed reactions, such as asymmetric hydrogenation and carbon-carbon bond formation, where it helps achieve high enantiomeric purity in the final products. Additionally, it is utilized in the development of chiral catalysts for industrial processes, enhancing the efficiency and selectivity of chemical transformations.

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Test Parameter Specification
Melting point 88-92
Purity (GC) 97-100%
Specific Rotation (A20/D C1 CHCl3) 112-123
Infrared Spectrometry Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,190.00
inventory 100mg
10-20 days ฿2,600.00
inventory 1g
10-20 days ฿19,250.00

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(R,R)-()-2,2'-Isopropylidenebis(4-tert-butyl-2-oxazoline)
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application extends to metal-catalyzed reactions, such as asymmetric hydrogenation and carbon-carbon bond formation, where it helps achieve high enantiomeric purity in the final p

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application extends to metal-catalyzed reactions, such as asymmetric hydrogenation and carbon-carbon bond formation, where it helps achieve high enantiomeric purity in the final products. Additionally, it is utilized in the development of chiral catalysts for industrial processes, enhancing the efficiency and selectivity of chemical transformations.

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