| Identification | More | [Name]
2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate | [CAS]
101385-69-7 | [Synonyms]
2-CHLORO-1,3-DIMETHYL-2-IMIDAZOLINIUM HEXAFLUOROPHOSPHATE 2-CHLORO-1,3-DIMETHYLIMIDAZOLIDINIUM HEXAFLUOROPHOSPHATE 2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM HEXAFLUOROPHOSPHATE 2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM PF6 CIP 2-Chlor-1,3-dimethyl-imidazolidinium-hexafluorophosphat 2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM HEXAFLUOROPHOSPHATE 98+% | [EINECS(EC#)]
628-484-4 | [Molecular Formula]
C5H12ClF6N2P | [MDL Number]
MFCD00191914 | [Molecular Weight]
280.58 | [MOL File]
101385-69-7.mol |
| Questions And Answer | Back Directory | [Synthesis]
Potassium hexafluorophosphate (1.32 g, 7.2 mmol) was added to a solution of 2-chloro-1,3-dimethyl-2-imidazolium chloride (1.24 g, 7.3 mmol) in dry acetonitrile (2 mL). The reaction mixture was then stirred at room temperature for 10 minutes. After the reaction was complete, the mixture was filtered through a diatomaceous earth filter to remove insoluble solids. The filtrate was then concentrated under vacuum, and the residue was dissolved in a small amount of acetonitrile (approximately 2 mL). The solution was then poured into diethyl ether, and a significant precipitate was observed to form in the reaction mixture. The precipitate was collected by vacuum filtration to obtain the target product, 2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate. Figure 2. Synthetic route of 2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate |
| Chemical Properties | Back Directory | [Melting point ]
231-233 °C (lit.) | [storage temp. ]
2-8°C
| [solubility ]
acetonitrile: 0.1 g/mL, clear
| [form ]
powder to crystal | [color ]
White to Almost white | [Sensitive ]
Moisture & Light Sensitive | [BRN ]
5369058 | [Major Application]
peptide synthesis | [InChI]
InChI=1S/C5H10ClN2.F6P/c1-7-3-4-8(2)5(7)6;1-7(2,3,4,5)6/h3-4H2,1-2H3;/q+1;-1 | [InChIKey]
CNAKHAGVVMOXFE-UHFFFAOYSA-N | [SMILES]
[P-](F)(F)(F)(F)(F)F.C1(Cl)=[N+](C)CCN1C | [CAS DataBase Reference]
101385-69-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Symbol(GHS) ]
 GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P264-P271-P280-P302+P352-P305+P351+P338 | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [F ]
8-10-21 | [HS Code ]
29332900 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Uses]
Reactant for synthesis of: Diazo-transfer reagents Reagent for synthesis of: Cannabinoid CB1 receptor agonists Selective small-molecule melanocortin-4 receptor agonists Imidazoles as selective cannabinoid CB2 receptor antagonists Cyclic alpha-peptoids Cyclic melanotropin peptide analogues selective for the human melanocortin-4 receptor | [General Description]
2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate is a reagent used for the coupling and esterification of sterically hindered amino acids.[1] | [reaction suitability]
reaction type: Coupling Reactions | [Solubility in organics]
2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate is soluble in DMF; partially soluble in H2O, MeOH, EtOAc, CH2Cl2, and CHCl3. | [storage]
2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate (CIP) can be stored refrigerated for at least 5 years without loss of reactivity. CIP is an irritant and should be used in a fumehood, when possible. | [References]
1. (a) Humphery, J. M.; Chamberlin, R., Chem. Rev. 1997, 97, 2243. (b) Albericio, F.; Carpino, L. A., Methods Enzymol. 1997, 289, 104 |
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