Bis[(pentamethylcyclopentadienyl)dichloro-rhodium]

Bis[(pentamethylcyclopentadienyl)dichloro-rhodium]

Min.Order / FOB Price:Get Latest Price

100 Kilogram	Negotiable

100 Kilogram

Negotiable

Min.Order :100 Kilogram
Purity: 99%
Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

RARECHEM AH PB 0251 12354-85-7 C20H30Cl4Rh2 10*

Quick Details

Appearance:powder
Application:12354-85-7
PackAge:Depended
ProductionCapacity:300|Kilogram|Month
Storage:Refrigerator
Transportation:by air or by sea

Superiority:

Bis[(pentamethylcyclopentadienyl)dichloro-rhodium] Basic information

Product Name:	Bis[(pentamethylcyclopentadienyl)dichloro-rhodium]
Synonyms:	Di-mu-chlorodichlorobis(pentamethyl-pi-cyclopentadienyl)dirhodium;Rhodium, di-mu-chlorodichlorobis[(1,2,3,4,5-eta)-1,2,3,4,5-pentamethyl-2,4-cyclopentadien-1-yl]di-;DI-MU-CHLORODICHLOROBIS-(PENTAMETHYLCYCLOPENTADIENYL)DIRHODATE;DICHLOROPENTAMETHYLCYCLOPENTADIENYLRHODIUM(III) DIMER;BIS[(PENTAMETHYLCYCLOPENTADIENYL)DICHLORO-RHODIUM];PENTAMETHYLCYCLOPENTADIENYLRHODIUM CHLORIDE DIMER;PENTAMETHYLCYCLOPENTADIENYLRHODIUM(III) CHLORIDE DIMER;PENTAMETHYLCYCLOPENTADIENYLRHODIUM(III)&
CAS:	12354-85-7
MF:	C20H30Cl4Rh2 10*
MW:	618.08
EINECS:
Product Categories:	Catalysts for Organic Synthesis;Classes of Metal Compounds;Homogeneous Catalysts;Metal Complexes;Rh (Rhodium) Compounds;Synthetic Organic Chemistry;Transition Metal Compounds;Catalysis and Inorganic Chemistry;Chemical Synthesis;Rhodium;metallocene;NULL
Mol File:	12354-85-7.mol

Bis[(pentamethylcyclopentadienyl)dichloro-rhodium] Chemical Properties

mp	>300°C
NIST Chemistry Reference	Rhodium, di-«mu»-chlorodichlorobis[(1,2,3,4,5-«eta»)-1,2,3,4,5-pentamethyl-2,4-cyclopentadien-1-yl]di-(12354-85-7)

Safety Information

Hazard Codes	Xn
Risk Statements	20/21/22-36/37/38-R36/37/38-R20/21/22
Safety Statements	26-36-S36-S26
WGK Germany	3

MSDS Information

Provider	Language
ACROS	English
SigmaAldrich	English
ALFA	English

Bis[(pentamethylcyclopentadienyl)dichloro-rhodium] Usage And Synthesis

Chemical Properties	burgundy solid
Usage	Oxidative olefination reactions C-C bond cleavage of secondary alcohols Ortho C-H olefination of phenol derivatives Oxidative annulation of pyridines Oxidative ortho-acylation of benzamides with aldehydes via direct functionalization of the sp2 C-H bond A

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