Cas 828917-29-9,ruthenium(II)(η3-2-C3H4Me)(CO)(benzyl isocyanide)(1,1'bis(diphenylphosphino)ferrocene)(SbF6)

828917-29-9

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Basic information

Product Name: ruthenium(II)(η3-2-C3H4Me)(CO)(benzyl isocyanide)(1,1'bis(diphenylphosphino)ferrocene)(SbF6)
Synonyms:
CAS NO:828917-29-9
Molecular Formula:
Molecular Weight: 1091.46
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: ruthenium(II)(η3-2-C3H4Me)(CO)(benzyl isocyanide)(1,1'bis(diphenylphosphino)ferrocene)(SbF6)(CAS DataBase Reference)
NIST Chemistry Reference: ruthenium(II)(η3-2-C3H4Me)(CO)(benzyl isocyanide)(1,1'bis(diphenylphosphino)ferrocene)(SbF6)(828917-29-9)
EPA Substance Registry System: ruthenium(II)(η3-2-C3H4Me)(CO)(benzyl isocyanide)(1,1'bis(diphenylphosphino)ferrocene)(SbF6)(828917-29-9)

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Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 828917-29-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 828917-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,8,9,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 828917-29:
(8*8)+(7*2)+(6*8)+(5*9)+(4*1)+(3*7)+(2*2)+(1*9)=209
209 % 10 = 9
So 828917-29-9 is a valid CAS Registry Number.

828917-29-9Upstream product

828917-29-9Downstream Products

828917-29-9Relevant academic research and scientific papers

[Ru(η3-2-C3H4Me)(CO)(dppf)][SbF 6]: A mononuclear 16e- ruthenium(II) catalyst for propargylic substitution and isomerization of HC≡CCPh2(OH)

Cadierno, Victorio,Diez, Josefina,Garcia-Garrido, Sergio E.,Gimeno, Jose

, p. 2716 - 2717 (2004)

The 16e- derivative [Ru(η3-2-C3H 4Me)(CO)(dppf][SbF6] catalyzes: (i) the propargylic substitution reaction of 1,1-diphenyl-2-propyn-1-ol with alcohols to produce propargylic ethers, and (ii) the formal isomerization of 1,1-diphenyl-2-propyn- 1-ol into 3,3-diphenyl-2-propenal.

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