Skip to Content
Merck
All Photos(3)

Documents

683094

Sigma-Aldrich

HS157

Umicore, 97%

Synonym(s):

Bis(1,5-cyclooctadiene)diiridium(I) dichloride, [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

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C16H24Cl2Ir2
CAS Number:
Molecular Weight:
671.70
EC Number:
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

powder

reaction suitability

core: iridium
reaction type: C-H Activation
reagent type: catalyst

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

Looking for similar products? Visit Product Comparison Guide

Application

Umicore Precatalysts for Asymmetric and Cross-Coupling Catalysis

Metal precursor for asymmetric allylic substitutions.

Legal Information

Product of Umicore

Additional information available at www.pmc.umicore.com

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Articles

Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.

Precatalysts for asymmetric catalysis offer batch-to-batch consistency in a range of catalytic reactions, supporting diverse research needs.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service