(R,R)-N-(p-Toluenesulfonyl)-1,2-diphenylethanediamine(chloro)(p-cymene)ruthenium(II)
95%
Reagent
Code: #70433
Alias
Chlorine {[(1R,2R)-(-)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)ammonia}(P-isopropyltoluene) RUTHENIUM (II) ) ruthenium ( II); Chloro[[(1R,2R)-(-)-2-amino-1,2-diphenylethyl](p-toluenesulfonyl)amino)](p-cymene)ruthenium(II); Chloro{[(1R,2R)-(-)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)ammonia}(P-isopropyltoluene)ruthenium(II))ruthenium( II); (R,R)-N-(p-toluenesulfonyl)-1,2-diphenylethanediamine (p-cymene) ruthenium(II) chloride
CAS Number
192139-92-7
blur_circular Chemical Specifications
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Molecular Information
Weight
636.219 g/mol
Formula
C₂₁H₂₁ClN₂O₂RuSC₁₀H₁₄
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Registry Numbers
MDL Number
MFCD10567385
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Physical Properties
Melting Point
215 °C
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Storage & Handling
Storage
2~8℃
description Product Description
This compound is primarily utilized in asymmetric catalysis, particularly in hydrogenation reactions. It is highly effective in producing chiral molecules, which are crucial in the pharmaceutical industry for the synthesis of enantiomerically pure drugs. The ruthenium complex facilitates the transfer of hydrogen atoms to prochiral substrates, enabling the formation of specific enantiomers with high selectivity. Its application extends to the production of fine chemicals and intermediates, where precise stereochemical control is essential. Additionally, it is employed in organic synthesis for the development of complex molecular structures with defined chiral centers, enhancing the efficiency and selectivity of synthetic routes.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Purity (HPLC) | 95-100% |
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