C78H64Cl5NO8P4Ru2
1646.6 g/mol
Research ReagentDanger
(NH2Me2)((RuCl((R)-segphos(regR)))2(mu-Cl)3)
CAS346457-41-8EC811-103-2
Category
Research Reagent
Compound Class
Organometallic
Primary Use
Research Compound
This compound is a dimethylammonium salt of a ruthenium(II) complex coordinated with bis(phosphine) ligands derived from benzodioxole. It is primarily used as a catalyst in asymmetric hydrogenation reactions.
Asymmetric hydrogenation catalyst
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
StrongSame Parent
Diacetato[(S)-(-)-5,5'-bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole]ruthenium(II)
CAS373650-12-5
research compound
StrongSame Parent
Dimethylammonium dichlorotri(mu-chloro)bis[(S)-(-)-5,5'-bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole]diruthenate(II)
CAS488809-34-3
research compound
StrongSame Parent
Chloro[(R)-(+)-5,5'-bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole](p-cymene)ruthenium(II) chloride
CAS944451-28-9
research compound
StrongSame Parent
Chloro[(S)-(-)-5,5'-bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole](p-cymene)ruthenium(II) chloride
CAS944451-29-0
research compound
ReferenceSame Category
4-Bromophenyl methyl sulfone
CAS3466-32-8
research compound
ReferenceSame Category
Dihydrotetrabenazine
CAS3466-75-9
research compound
ReferenceSame Category
3-methylflavone-8-carboxylic acid
CAS3468-01-7
research compound
ReferenceSame Category
2,7-Dimethoxynaphthalene
CAS3469-26-9
research compound
Safety Reference
Danger
H360May damage fertility or the unborn child
H371May cause damage to organs
H373May cause damage to organs through prolonged or repeated exposure
Identifiers
IUPAC Name
dimethylazanium;bis([4-(5-diphenylphosphanyl-1,3-benzodioxol-4-yl)-1,3-benzodioxol-5-yl]-diphenylphosphane);bis(ruthenium(2+));pentachloride
InChIKey
RSZXAODKXNGMHV-UHFFFAOYSA-J
SMILES
C[NH2+]C.C1OC2=C(O1)C(=C(C=C2)P(C3=CC=CC=C3)C4=CC=CC=C4)C5=C(C=CC6=C5OCO6)P(C7=CC=CC=C7)C8=CC=CC=C8.C1OC2=C(O1)C(=C(C=C2)P(C3=CC=CC=C3)C4=CC=CC=C4)C5=C(C=CC6=C5OCO6)P(C7=CC=CC=C7)C8=CC=CC=C8.[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Ru+2].[Ru+2]
Synonyms (3)
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