(1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)cyclohexane-1,2-diamine

97%

Reagent Code: #126734
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Alias (1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)-1,2-cyclohexanediamine (1S,2S)-N,N'-1,2 -Cyclohexanediylbis[N-hydroxy-α-phenyl-phenylacetamide]
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CAS Number 1217464-22-6

science Other reagents with same CAS 1217464-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 534.66 g/mol
Formula C₃₄H₃₄N₂O₄
badge Registry Numbers
MDL Number MFCD11044410
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its structure, featuring multiple functional groups, makes it effective in asymmetric synthesis, particularly in reactions that require high enantioselectivity. It is often employed in the formation of carbon-carbon or carbon-heteroatom bonds, aiding in the production of complex molecules with specific stereochemistry. Additionally, its ability to coordinate with metal ions enhances its use in metal-catalyzed reactions, contributing to the development of pharmaceuticals, agrochemicals, and fine chemicals. Its stability and selectivity make it a valuable tool in advanced synthetic chemistry applications.

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Test Parameter Specification
Appearance White to light yellow to light orange powder to crystal
Purity (%) 95.0-96.5
Specific Rotation [A]20/D (C=1, CHCl3) -95.0 to -85.0
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,690.00

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(1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)cyclohexane-1,2-diamine
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This compound is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its structure, featuring multiple functional groups, makes it effective in asymmetric synthesis, particularly in reactions that require high enantioselectivity. It is often employed in the formation of carbon-carbon or carbon-heteroatom bonds, aiding in the production of complex molecules with specific stereochemistry. Additionally, its ability to coordinate with metal ions enhances its use in metal-cata

This compound is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its structure, featuring multiple functional groups, makes it effective in asymmetric synthesis, particularly in reactions that require high enantioselectivity. It is often employed in the formation of carbon-carbon or carbon-heteroatom bonds, aiding in the production of complex molecules with specific stereochemistry. Additionally, its ability to coordinate with metal ions enhances its use in metal-catalyzed reactions, contributing to the development of pharmaceuticals, agrochemicals, and fine chemicals. Its stability and selectivity make it a valuable tool in advanced synthetic chemistry applications.

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