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715417

Sigma-Aldrich

1,3-Bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene

Synonym(s):

1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene, SIMes

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About This Item

Empirical Formula (Hill Notation):
C21H26N2
CAS Number:
173035-11-5
Molecular Weight:
306.44
MDL number:
MFCD11973794
UNSPSC Code:
12352005
PubChem Substance ID:
329762968
NACRES:
NA.22

form

powder

reaction suitability

reagent type: catalyst

mp

79-85 °C

storage temp.

−20°C

SMILES string

Cc1cc(C)c(N2[C]N(CC2)c3c(C)cc(C)cc3C)c(C)c1

InChI

1S/C21H26N2/c1-14-9-16(3)20(17(4)10-14)22-7-8-23(13-22)21-18(5)11-15(2)12-19(21)6/h9-12H,7-8H2,1-6H3

InChI key

LSMWOQFDLBIYPM-UHFFFAOYSA-N

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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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Hao Mei et al.
BMC genomics, 16, 336-336 (2015-04-23)
Genetic heritability and expression study have shown that different diabetes traits have common genetic components and pathways. A computationally efficient pathway analysis of GWAS results will benefit post-GWAS study of SNP associations and identification of common genetic pathways from diabetes

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1-tBu-Indenyl Supported Palladium Precatalysts for Cross-Coupling

The Hazari group has developed an improved palladium precatalyst scaffold for a wide range of cross-coupling reactions

1-tBu-Indenyl Supported Palladium Precatalysts for Cross-Coupling

The Hazari group has developed an improved palladium precatalyst scaffold for a wide range of cross-coupling reactions

1-tBu-Indenyl Supported Palladium Precatalysts for Cross-Coupling

The Hazari group has developed an improved palladium precatalyst scaffold for a wide range of cross-coupling reactions

1-tBu-Indenyl Supported Palladium Precatalysts for Cross-Coupling

The Hazari group has developed an improved palladium precatalyst scaffold for a wide range of cross-coupling reactions

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