661023
Hydroxy(cyclooctadiene)rhodium(I) dimer
95%
Synonym(s):
(Cyclooctadiene)rhodium hydroxide dimer, 1,5-Cyclooctadiene)hydroxyrhodium dimer, Bis(cyclooctadiene)dihydroxodirhodium, Bis[(1,2,5,6-η)-1,5-cyclooctadiene]di--μ-hydroxydirhodium, Bis[(1,5-cyclooctadiene)(hydroxy)rhodium], [Rh(OH)(1,5-cod)]2
About This Item
Quality Level
Assay
95%
form
solid
reaction suitability
core: rhodium
reagent type: catalyst
greener alternative product characteristics
Catalysis
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Greener Alternative Product
mp
199 °C (dec.)
greener alternative category
SMILES string
O[Rh].O[Rh].C1CC=CCCC=C1.C2CC=CCCC=C2
InChI
1S/2C8H12.2H2O.2Rh/c2*1-2-4-6-8-7-5-3-1;;;;/h2*1-2,7-8H,3-6H2;2*1H2;;/q;;;;2*+1/p-2/b2*2-1-,8-7-;;;;
InChI key
IUAQXTGDGDIMOD-MIXQCLKLSA-L
General description
Application
Rhodium-Catalyzed Oxygenative Addition to Terminal Alkynes for the Synthesis of Esters, Amides, and Carboxylic Acids
Legal Information
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
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Articles
Discover the role of boronic acids in enantioenriched C(sp2)–C(sp2) product synthesis, specifically the rhodium-catalyzed Suzuki–Miyaura-type arylations of allylic halides and cyclobutenes.
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