Cas 749926-38-3,ruthenium Cl<sub>2</sub> (eta.6-hexamethylbenzene)[N-(2,4,6-trimethylbenzyl)benzimidazole]

749926-38-3

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Basic information

Product Name: ruthenium Cl₂ (eta.6-hexamethylbenzene)[N-(2,4,6-trimethylbenzyl)benzimidazole]
Synonyms:
CAS NO:749926-38-3
Molecular Formula:
Molecular Weight: 584.594
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 Cl₂ (eta.6-hexamethylbenzene)[N-(2,4,6-trimethylbenzyl)benzimidazole](CAS DataBase Reference)
NIST Chemistry Reference: ruthenium Cl₂ (eta.6-hexamethylbenzene)[N-(2,4,6-trimethylbenzyl)benzimidazole](749926-38-3)
EPA Substance Registry System: ruthenium Cl₂ (eta.6-hexamethylbenzene)[N-(2,4,6-trimethylbenzyl)benzimidazole](749926-38-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 749926-38-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 749926-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,9,9,2 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 749926-38:
(8*7)+(7*4)+(6*9)+(5*9)+(4*2)+(3*6)+(2*3)+(1*8)=223
223 % 10 = 3
So 749926-38-3 is a valid CAS Registry Number.

749926-38-3Upstream product

749926-38-3Downstream Products

749926-38-3Relevant academic research and scientific papers

Access to 3-Methyl-4-methylene-N-tosylpyrrolidine and 3,4-Dimethyl-N-tosylpyrroline by Ruthenium-Catalyzed Cascade Cycloisomerization/Isomerization Reactions

Oezdemir, Ismail,Cetinkaya, Engin,Cetinkaya, Bekir,Cicek, Metin,Semeril, David,Bruneau, Christian,Dixneuf, Pierre H.

, p. 418 - 422 (2004)

New RuCl2(benzimidazole)(arene) complexes have been prepared. Upon reaction with 1,1-diphenylprop-2-ynol they generate catalyst precursors which perform the cycloisomerization of diallyltosylamide into 3-methyl-4-methylene-N-tosylpyrrolidine. T

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