420336
2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate
98%
Synonym(s):
2-Chloro-4,5-dihydro-1,3-dimethyl-1H-imidazolium hexafluorophosphate, CIP
About This Item
Quality Level
Assay
98%
reaction suitability
reaction type: Coupling Reactions
mp
231-233 °C (lit.)
application(s)
peptide synthesis
SMILES string
F[P-](F)(F)(F)(F)F.CN1CC[N+](C)=C1Cl
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
InChI key
CNAKHAGVVMOXFE-UHFFFAOYSA-N
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Related Categories
Application
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
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Articles
N-Acylimidazoles and carbonylimidazoles are reactive intermediates used for amino compound acylation, surpassing DCC as coupling reagents.
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