1,3-Di(pyridin-2-yl)benzene

97%

Reagent Code: #178128
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CAS Number 136538-84-6

science Other reagents with same CAS 136538-84-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.28 g/mol
Formula C₁₆H₁₂N₂
badge Registry Numbers
MDL Number MFCD14584756
thermostat Physical Properties
Boiling Point 401.2±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.125±0.06 g/cm3(Predicted)
Storage Room temperature, inert gas

description Product Description

Used as a ligand in coordination chemistry, particularly in the design of transition metal complexes for catalysis. Its structure allows for chelation with metals, enhancing stability and reactivity in catalytic reactions. Commonly applied in homogeneous catalysis, including C–H activation and cross-coupling reactions. Also explored in the development of luminescent materials and sensors due to its ability to form complexes with lanthanides and other emissive metal centers. Its rigid aromatic framework supports the construction of metal-organic frameworks (MOFs) and supramolecular architectures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,360.00
250mg
10-20 days ฿4,720.00
1g
10-20 days ฿11,380.00
5g
10-20 days ฿47,770.00
1,3-Di(pyridin-2-yl)benzene
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Used as a ligand in coordination chemistry, particularly in the design of transition metal complexes for catalysis. Its structure allows for chelation with metals, enhancing stability and reactivity in catalytic reactions. Commonly applied in homogeneous catalysis, including C–H activation and cross-coupling reactions. Also explored in the development of luminescent materials and sensors due to its ability to form complexes with lanthanides and other emissive metal centers. Its rigid aromatic framework supp
Used as a ligand in coordination chemistry, particularly in the design of transition metal complexes for catalysis. Its structure allows for chelation with metals, enhancing stability and reactivity in catalytic reactions. Commonly applied in homogeneous catalysis, including C–H activation and cross-coupling reactions. Also explored in the development of luminescent materials and sensors due to its ability to form complexes with lanthanides and other emissive metal centers. Its rigid aromatic framework supports the construction of metal-organic frameworks (MOFs) and supramolecular architectures.
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