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Merck
CN

661023

Hydroxy(cyclooctadiene)rhodium(I) dimer

greener alternative

95%, solid

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

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About This Item

Empirical Formula (Hill Notation):
C16H26O2Rh2
CAS Number:
73468-85-6
Molecular Weight:
456.19
UNSPSC Code:
12161600
PubChem Substance ID:
24884496
NACRES:
NA.22
MDL number:
MFCD08457638

Key Documents

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Product Name

Hydroxy(cyclooctadiene)rhodium(I) dimer, 95%

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

assay

95%

form

solid

reaction suitability

core: rhodium, reagent type: catalyst

greener alternative product characteristics

Catalysis
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sustainability

Greener Alternative Product

mp

199 °C (dec.)

greener alternative category

Aligned,

Quality Level

100

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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. Click here for more information.

Application

Efficient and Selective Catalysts for Asymmetric Synthesis
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
Rhodium catalyst employed with R-BINAP or R-SEGPHOS® ligands in a synthesis of chiral 3,3-disubstituted-1-indanones.

Legal Information

SEGPHOS is a registered trademark of Takasago Intl. Corp.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SHBR7451
SHBQ3477
SHBN6733
SHBJ7819
SHBJ2033

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Rhodium-catalyzed asymmetric synthesis of 3,3-disubstituted 1-indanones.
Ryo Shintani et al.
Angewandte Chemie (International ed. in English), 46(20), 3735-3737 (2007-04-05)

Articles

Rhodium Catalyzed Asymmetric Suzuki Related Cross Coupling Reactions

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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