275131
Bis(1,5-cyclooctadiene)diiridium(I) dichloride
97%
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Synonym(s):
[Ir(1,5-cod)Cl]2, 1,5-Cyclooctadiene-iridium(I) chloride dimer, Chloro(1,5-cyclooctadiene)iridium(I) dimer, Di-μ-chlorobis[(1,2,5,6-η)-1,5-cyclooctadiene]diiridium, Iridium(I) chloride 1,5-cyclooctadiene complex dimer, [Ir(1,5-cod)Cl]2, [Ir(cod)Cl]2
Empirical Formula (Hill Notation):
C16H24Cl2Ir2
CAS Number:
Molecular Weight:
671.70
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
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Assay
97%
reaction suitability
reagent type: catalyst
core: iridium
mp
205 °C (dec.) (lit.)
SMILES string
Cl[Ir].Cl[Ir].C1CC=CCCC=C1.C2CC=CCCC=C2
InChI
1S/2C8H12.2ClH.2Ir/c2*1-2-4-6-8-7-5-3-1;;;;/h2*1-2,7-8H,3-6H2;2*1H;;/q;;;;2*+1/p-2/b2*2-1-,8-7-;;;;
InChI key
ZFOUDQNHNLDNLD-MIXQCLKLSA-L
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Application
Metal precursor for asymmetric allylic substitutions.
Regulatory Information
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P A Marks et al.
Journal of the National Cancer Institute, 92(15), 1210-1216 (2000-08-03)
Histone deacetylase (HDAC) inhibitors have been shown to be potent inducers of growth arrest, differentiation, and/or apoptotic cell death of transformed cells in vitro and in vivo. One class of HDAC inhibitors, hydroxamic acid-based hybrid polar compounds (HPCs), induce differentiation
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