1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride
97%
- Product Code: 69002
Alias:
1,3-bis(2,6-diisopropylphenyl) imidazole chloride
CAS:
250285-32-6
Molecular Weight: | 425.05 g./mol | Molecular Formula: | C₂₇H₃₇ClN₂ |
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EC Number: | MDL Number: | MFCD02684545 | |
Melting Point: | 278 °C (dec.)(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8℃, dry, sealed |
Product Description:
This chemical is widely used as a precursor in the synthesis of N-heterocyclic carbenes (NHCs), which are essential ligands in organometallic chemistry. These ligands play a crucial role in stabilizing transition metal complexes, particularly in catalytic processes such as olefin metathesis, hydrogenation, and cross-coupling reactions. Its sterically bulky structure enhances the stability and reactivity of the resulting metal complexes, making it valuable in industrial and academic research. Additionally, it finds applications in the development of ionic liquids and as a catalyst in organic synthesis, contributing to advancements in green chemistry and sustainable processes.
Product Specification:
Test | Specification |
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ELEMENTAL ANALYSIS | 73.6-79 |
PURITYHPLC | 97-100 |
APPEARANCE | White to Light yellow to Orange to Brown Powder, Crystals, Crystalline Powder and/or Chunks |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $18.32 |
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1.000 | 10-20 days | $38.51 |
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5.000 | 10-20 days | $150.28 |
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25.000 | 10-20 days | $717.61 |
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1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride
This chemical is widely used as a precursor in the synthesis of N-heterocyclic carbenes (NHCs), which are essential ligands in organometallic chemistry. These ligands play a crucial role in stabilizing transition metal complexes, particularly in catalytic processes such as olefin metathesis, hydrogenation, and cross-coupling reactions. Its sterically bulky structure enhances the stability and reactivity of the resulting metal complexes, making it valuable in industrial and academic research. Additionally, it finds applications in the development of ionic liquids and as a catalyst in organic synthesis, contributing to advancements in green chemistry and sustainable processes.
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