| Identification | Back Directory | [Name]
Umicore M2 | [CAS]
536724-67-1 | [Synonyms]
NEOLYST M2
Umicore M 2
NEOLYST(TM) M2
UMicore M2, 10% Ru, Product of UMicore
Dichloro(1,3-dimesityl-2-imidazolidinylidene)(3-phenyl-1H-inden-1-ylidene)ruthenium-tricyclohexylphosphine (1:1)
TRICYCLOHEXYLPHOSPHINE[3- PHENYL-1H-INDEN-1-YLIDENE][1,3- BIS(2,4,6-TRIMETHYLPHENYL)-4,5- dihydroimidazol-2-ylidene]Ru(II)Cl2
1,3-BIS(2,4,6-TRIMETHYLPHENYL)-2-IMIDAZOLIDINYLIDENE]DICHLORO(3-PHENYL-1H-INDEN-1-YLIDENE)(TRICYCLOHEXYLPHOSPHINE)RUTHENIUM(II)
Dichloro[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene](3-phenyl-1H-inden-1-ylidene)(tricyclohexylphosphine)ruthenium(II)
Tricyclohexylphosphine[3-phenyl-1H-inden-1-ylidene][1,3-bis(2,4,6-triMethylphenyl)-4,5-dihydroiMidazol-2-ylidene]rutheniuM(II),95%
(SP-5-41)-[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(3-phenyl-1H-inden-1-ylidene)(tricyclohexylphosphine)ruthenium
TRICYCLOHEXYLPHOSPHINE[3-PHENYL-1H-INDEN-1-YLIDENE][1,3-BIS(2,4,6-TRIMETHYLPHENYL)-4,5-DIHYDROIMIDAZOL-2-YLIDENE]RUTHENIUM (II) DICHLORIDE
RutheniuM, [1,3-bis(2,4,6-triMethylphenyl)-2-iMidazolidinylidene]dichloro(3-phenyl-1H-inden-1-ylidene)(tricyclohexylphosphine)-, (SP-5-41)-
Tricyclohexylphosphine[3-phenyl-1H-inden-1-ylidene][1,3-bis(2,4,6-trimethylphenyl)-4,5dihydroimidazol-2- ylidene]ruthenium(II)dichloride,min.95%
Tricyclohexylphosphine[3-phenyl-1H-inden-1-ylidene][1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene]ruthenium(II) dichloride, min. 95%
Tricyclohexylphosphine[3-phenyl-1H-inden-1-ylidene][1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene]ruthenium(II)dichloride,min.95%NeolystM2
Tricyclohexylphosphine[3-phenyl-1H-inden-1-ylidene][1,3-bis(2,4,6-
trimethylphenyl)-4,5-dihydroimidazol-2-ylidene]ruthenium (II) dichloride, min. 95% | [Molecular Formula]
C36H36Cl2N2Ru.C18H33P | [MDL Number]
MFCD08667892 | [MOL File]
536724-67-1.mol | [Molecular Weight]
949.103 |
| Hazard Information | Back Directory | [Chemical Properties]
Red powder | [Uses]
Neolyst Dichloride acts as a catalyst in cross-metathesis reactions. In addition it is used in the preparation of Weinreb amide pyrrolidines. |
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