2,6-Dibenzhydryl-2,6-diazaspiro[3.3]heptane

95%

Reagent Code: #75105
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CAS Number 913814-37-6

science Other reagents with same CAS 913814-37-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 430.6 g/mol
Formula C₃₁H₃₀N₂
badge Registry Numbers
MDL Number MFCD13180718
thermostat Physical Properties
Boiling Point 533.4℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.19g/ml
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a ligand in catalytic processes. Its unique spirocyclic structure and the presence of dibenzhydryl groups make it highly effective in stabilizing metal complexes, which are crucial for various catalytic reactions. It is often employed in polymerization reactions, where it helps in controlling the molecular weight and distribution of polymers. Additionally, its steric and electronic properties make it suitable for use in asymmetric catalysis, enabling the production of chiral molecules with high enantioselectivity. This chemical is also explored in the development of advanced materials, where its structural features contribute to the design of novel polymers and catalysts with tailored properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿95,490.00
inventory 1g
10-20 days ฿235,520.00

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2,6-Dibenzhydryl-2,6-diazaspiro[3.3]heptane
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This compound is primarily utilized in the field of organic synthesis, particularly as a ligand in catalytic processes. Its unique spirocyclic structure and the presence of dibenzhydryl groups make it highly effective in stabilizing metal complexes, which are crucial for various catalytic reactions. It is often employed in polymerization reactions, where it helps in controlling the molecular weight and distribution of polymers. Additionally, its steric and electronic properties make it suitable for use i

This compound is primarily utilized in the field of organic synthesis, particularly as a ligand in catalytic processes. Its unique spirocyclic structure and the presence of dibenzhydryl groups make it highly effective in stabilizing metal complexes, which are crucial for various catalytic reactions. It is often employed in polymerization reactions, where it helps in controlling the molecular weight and distribution of polymers. Additionally, its steric and electronic properties make it suitable for use in asymmetric catalysis, enabling the production of chiral molecules with high enantioselectivity. This chemical is also explored in the development of advanced materials, where its structural features contribute to the design of novel polymers and catalysts with tailored properties.

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