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420336

Sigma-Aldrich

2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate

98%

Synonym(s):

2-Chloro-4,5-dihydro-1,3-dimethyl-1H-imidazolium hexafluorophosphate, CIP

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About This Item

Empirical Formula (Hill Notation):
C5H10ClF6N2P
CAS Number:
Molecular Weight:
278.56
Beilstein:
5369058
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

reaction suitability

reaction type: Coupling Reactions

mp

231-233 °C (lit.)

application(s)

peptide synthesis

functional group

chloro

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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Application

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Articles

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N-Acylimidazoles and carbonylimidazoles are reactive intermediates used for amino compound acylation, surpassing DCC as coupling reagents.

N-Acylimidazoles and carbonylimidazoles are reactive intermediates used for amino compound acylation, surpassing DCC as coupling reagents.

N-Acylimidazoles and carbonylimidazoles are reactive intermediates used for amino compound acylation, surpassing DCC as coupling reagents.

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