Cas 191427-11-9,(CH3OC6H3P(C6H3(C(CH3)3)2)2)2RuHC3H7C6H4CH3(1+)*BF4(1-) = [(CH3OC6H3P(C14H21)2)2RuHC10H14][BF4]

191427-11-9

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Product Name: (CH₃OC₆H₃P(C₆H₃(C(CH₃)3)2)2)2RuHC₃H₇C₆H₄CH₃⁽¹⁺⁾*BF₄^(1-) = [(CH₃OC₆H₃P(C₁₄H₂₁)2)2RuHC₁₀H₁₄][BF₄]
Synonyms:
CAS NO:191427-11-9
Molecular Formula:
Molecular Weight: 1354.58
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (CH₃OC₆H₃P(C₆H₃(C(CH₃)3)2)2)2RuHC₃H₇C₆H₄CH₃⁽¹⁺⁾*BF₄^(1-) = [(CH₃OC₆H₃P(C₁₄H₂₁)2)2RuHC₁₀H₁₄][BF₄](CAS DataBase Reference)
NIST Chemistry Reference: (CH₃OC₆H₃P(C₆H₃(C(CH₃)3)2)2)2RuHC₃H₇C₆H₄CH₃⁽¹⁺⁾*BF₄^(1-) = [(CH₃OC₆H₃P(C₁₄H₂₁)2)2RuHC₁₀H₁₄][BF₄](191427-11-9)
EPA Substance Registry System: (CH₃OC₆H₃P(C₆H₃(C(CH₃)3)2)2)2RuHC₃H₇C₆H₄CH₃⁽¹⁺⁾*BF₄^(1-) = [(CH₃OC₆H₃P(C₁₄H₂₁)2)2RuHC₁₀H₁₄][BF₄](191427-11-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 191427-11-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 191427-11-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,4,2 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 191427-11:
(8*1)+(7*9)+(6*1)+(5*4)+(4*2)+(3*7)+(2*1)+(1*1)=129
129 % 10 = 9
So 191427-11-9 is a valid CAS Registry Number.

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191427-11-9Relevant academic research and scientific papers

Enantioselective homogeneous catalysis and the '3,5-dialkyl meta- effect'. MeO-BIPHEP complexes related to heck, allylic alkylation, and hydrogenation chemistry

Trabesinger, Gerald,Albinati, Alberto,Feiken, Nantko,Kunz, Roland W.,Pregosin, Paul S.,Tschoerner, Matthias

, p. 6315 - 6323 (2007/10/03)

The enantioselectivities arising from a Pd-catalyzed Heck reaction (>98% ee) and an allylic alkylation (>90% ee) using a 3,5-di-tert-butyl-MeO-BIPHEP chiral auxiliary (1) are reported. Higher ee's are observed with the 3,5- dialkyl substituents than with

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