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CAS RN: 917604-39-8 | Product Number: B5603
1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate
Purity: >98.0%(T)(HPLC)
Synonyms:
- IPr·CO2
Product Documents:
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1G |
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Product Number | B5603 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__2__8H__3__6N__2O__2 = 432.61 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Hygroscopic |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
CAS RN | 917604-39-8 |
Reaxys Registry Number | 9656270 |
PubChem Substance ID | 354335706 |
Specifications
Appearance | White to Almost white powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Nonaqueous Titration) | min. 98.0 % |
Properties (reference)
Melting Point | 198 °C(dec.) |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
H.S.code* | 2933.29-000 |
Application
Gold Surface Modification with N-Heterocyclic Carbene
Reference
- Ballbot-type motion of N-heterocyclic carbenes on gold surfaces
Application
NHC-CO2 Adducts: Transition Metal / NHC Complex Catalyst Preparation
A mixture of [Rh(cod)Cl]2 (54 mg) and NHC-CO2 adduct (2 eq.) is stirred in acetonitrile (3 ml) for 5 min at room temperature in a Schlenk flask, followed by heating at 75 °C for 20 min under an atmosphere of argon. The reaction mixture is dried in vacuo, and washed three times with diethyl ether. The yellow solid obtained is analytically pure (93%).
References
- Disubstituted Imidazolium-2-Carboxylates as Efficient Precursors to N-Heterocyclic Carbene Complexes of Rh, Ru, Ir, and Pd
Application
Conjugate Cyanation using NHC-CO2 Adducts as a Precursor to NHC Catalysts
Reference
- N-Heterocyclic Carbene Catalyzed 1,6-Conjugate Addition of Me3Si-CN to para-Quinone Methides and Fuchsones: Access to α-Arylated Nitriles
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