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756369

Sigma-Aldrich

1,3-Dicyclohexylimidazolium chloride

Synonym(s):

1,3-Dicyclohexyl-1H-imidazolium chloride

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About This Item

Empirical Formula (Hill Notation):
C15H25ClN2
CAS Number:
181422-72-0
Molecular Weight:
268.83
MDL number:
MFCD04973309
UNSPSC Code:
12352005
PubChem Substance ID:
329766536
NACRES:
NA.22

form

solid

reaction suitability

reagent type: catalyst

mp

101-144 °C (decomposition)

SMILES string

[Cl-].C1CCC(CC1)n2cc[n+](c2)C3CCCCC3

InChI

1S/C15H25N2.ClH/c1-3-7-14(8-4-1)16-11-12-17(13-16)15-9-5-2-6-10-15;/h11-15H,1-10H2;1H/q+1;/p-1

InChI key

UPJKDKOHHMKJAY-UHFFFAOYSA-M

Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Rimesh Augustine et al.
Journal of materials chemistry. B, 8(26), 5745-5755 (2020-06-11)
A series of multi-stimuli-responsive poly(N-isopropylacrylamide)30-SS-block-poly(L-lysine)30-block-poly(caprolactone)n (p(NIPAM)30-SS-b-p(Lys)30-b-p(CL)n) (n = 50, 75, 100, 125) triblock copolymers have been synthesized by combining reversible addition-fragmentation chain transfer polymerization of NIPAM, organo-catalyzed ring-opening polymerization (ROP) of Z-lysine N-carboxyanhydride and metal-catalyzed ROP of CL with an

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