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Merck
CN

938726

ImPy-Dipop-Dipp

greener alternative

powder

Synonym(s):

5-(2,6-diisopropoxyphenyl)-2-(2,6-diisopropylphenyl)imidazo[1,5-a]pyridin-2-ium chloride

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About This Item

Empirical Formula (Hill Notation):
C31H39ClN2O2
CAS Number:
Molecular Weight:
507.11
UNSPSC Code:
12352100
NACRES:
NA.21
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Product Name

ImPy-Dipop-Dipp,

InChI

1S/C31H39N2O2.ClH/c1-20(2)25-13-10-14-26(21(3)4)31(25)32-18-24-12-9-15-27(33(24)19-32)30-28(34-22(5)6)16-11-17-29(30)35-23(7)8;/h9-23H,1-8H3;1H/q+1;/p-1

InChI key

XMDMIAJKGFBECK-UHFFFAOYSA-M

SMILES string

CC(C1=CC=CC(C(C)C)=C1[N+]2=CN3C(C4=C(OC(C)C)C=CC=C4OC(C)C)=CC=CC3=C2)C.[Cl-]

form

powder

reaction suitability

reaction type: Cross Couplings

greener alternative product characteristics

Catalysis
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color

white

greener alternative category

Quality Level

General description

ImPy-Dipop-Dipp is an NHC precursor developed in the Szostak group. The ligand is useful in a range of catalytic transformations, and is particulary well suited to the following: Suzuki-Miyaura cross-coupling of aryl mesylates and tosylates, Suzuki–Miyaura cross-coupling of nitroarenes (Ar–NO2), Buchwald-Hartwig amination of alkyl sulfoxides
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Application

Suzuki-Miyaura cross-coupling of aryl mesylates and tosylates Suzuki–Miyaura cross-coupling of nitroarenes (Ar–NO2) or aryl sulfamates Buchwald-Hartwig amination of alkyl sulfoxides or aryl sulfamates

Features and Benefits

ImPy-Dipop-Dipp is an asymmetric NHC ligand precursor. It forms air-and moisture stable complexes with transition metals and is particulary effective in palladium catalyzed cross-coupling reactions.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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