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Home/Compounds/Research Reagent/Chloro[[(1S,2S)-(+)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido](mesitylene)ruthenium(II)
C30H33ClN2O2RuS
622.2 g/mol
Research ReagentDanger

((1S,2S)-2-amino-1,2-diphenylethyl)[(4-methylphenyl)sulfonyl]amine ruthenium chloride 1,3,5-trimethylbenzene complex

CAS174813-81-1EC692-000-8
Category
Research Reagent
Compound Class
Organometallic
Primary Use
Research Compound

This compound is a ruthenium-based asymmetric hydrogenation catalyst, commonly used in research laboratories for enantioselective synthesis. Its structure features a chiral sulfonylazanide ligand coordinated to ruthenium, along with mesitylene as a stabilizing ligand.

asymmetric hydrogenation catalyst for enantioselective synthesisresearch reagent for catalytic studies

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

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Referencestereoisomer of

Chloro[[(1R,2R)-(-)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido](mesitylene)ruthenium(II)

CAS174813-82-2

research compound

Referencesame scaffold

Chloro[[(1S,2S)-(+)-2-amino-1,2-diphenylethyl](pentafluorophenylsulfonyl)amido](p-cymene)ruthenium(II)

CAS1026995-72-1

research compound

Safety Reference

Flammable
Flammable
Harmful
Harmful
Health Hazard
Health Hazard
Environmental Hazard
Environmental Hazard
Danger
H228Flammable solid
H302Harmful if swallowed
H315Causes skin irritation
H317May cause an allergic skin reaction
H319Causes serious eye irritation
H335May cause respiratory irritation
H361Suspected of damaging fertility or the unborn child
H371May cause damage to organs
H400Very toxic to aquatic life
H410Very toxic to aquatic life with long lasting effects
Identifiers
IUPAC Name

[(1S,2S)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1,3,5-trimethylbenzene

InChIKey

XBNBOGZUDCYNOJ-XCPIVNJJSA-M

SMILES

CC1=CC=C(C=C1)S(=O)(=O)[N-][C@@H](C2=CC=CC=C2)[C@H](C3=CC=CC=C3)N.CC1=CC(=CC(=C1)C)C.Cl[Ru+]

Synonyms (5)

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