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Merck
CN

227951

Chloro(1,5-cyclooctadiene)rhodium(I) dimer

greener alternative

98%, solid

Synonym(s):

1,5-Cyclooctadienerhodium(I) chloride dimer, Bis(1,5-cyclooctadiene)dirhodium(I) dichloride, Di-μ-chlorobis[(1,2,5,6-η)-1,5-cyclooctadiene]dirhodium, Rhodium(I) chloride 1,5-Cyclooctadiene complex dimer, [Rh(COD)Cl]2

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About This Item

Empirical Formula (Hill Notation):
C16H24Cl2Rh2
CAS Number:
Molecular Weight:
493.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
235-157-6
MDL number:
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Product Name

Chloro(1,5-cyclooctadiene)rhodium(I) dimer, 98%

Quality Level

assay

98%

form

solid

reaction suitability

core: rhodium, reagent type: catalyst

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

243 °C (dec.) (lit.)

greener alternative category

SMILES string

Cl[Rh].Cl[Rh].C1CC=CCCC=C1.C2CC=CCCC=C2

InChI

1S/2C8H12.2ClH.2Rh/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

QSUDXYGZLAJAQU-MIXQCLKLSA-L

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Find details here.

Application

Catalyst for coupling 1,3-dienes with activated hydrocarbons and for preparing chiral complexes.
Catalyst for oxygenative addition to terminal alkynes for a greener synthesis esters, amides, and carboxylic acids.

Rhodium-Catalyzed Oxygenative Addition to Terminal Alkynes for the Synthesis of Esters, Amides, and Carboxylic Acids


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Tetrahedron Asymmetry, 4, 2279-2279 (1993)
Fung Kei Cheung et al.
Organic & biomolecular chemistry, 5(7), 1093-1103 (2007-03-23)
A series of catalysts have been prepared for use in the asymmetric transfer hydrogenation of ketones. The complexes were prepared using a [4 + 2] cycloaddition reaction at a key step in the reaction sequence. This provides a means for
Pure and Applied Chemistry. Chimie Pure Et Appliquee, 66, 1509-1509 (1994)



Global Trade Item Number

SKUGTIN
227951-500MG04061838781048
227951-50G04061833410363
227951-5G04061838781055