Cas 909791-75-9,2-(2,3,4,5-tetramethylcyclopentadienyl)-benzyl (1R,2R)-p-toluenesulfonyl-cyclohexyldiamine

909791-75-9

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Basic information

Product Name: 2-(2,3,4,5-tetramethylcyclopentadienyl)-benzyl (1R,2R)-p-toluenesulfonyl-cyclohexyldiamine
Synonyms: 2-(2,3,4,5-tetramethylcyclopentadienyl)-benzyl (1R,2R)-p-toluenesulfonyl-cyclohexyldiamine
CAS NO:909791-75-9
Molecular Formula:
Molecular Weight: 478.699
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: 2-(2,3,4,5-tetramethylcyclopentadienyl)-benzyl (1R,2R)-p-toluenesulfonyl-cyclohexyldiamine(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2,3,4,5-tetramethylcyclopentadienyl)-benzyl (1R,2R)-p-toluenesulfonyl-cyclohexyldiamine(909791-75-9)
EPA Substance Registry System: 2-(2,3,4,5-tetramethylcyclopentadienyl)-benzyl (1R,2R)-p-toluenesulfonyl-cyclohexyldiamine(909791-75-9)

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: 909791-75-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 909791-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,7,9 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 909791-75:
(8*9)+(7*0)+(6*9)+(5*7)+(4*9)+(3*1)+(2*7)+(1*5)=219
219 % 10 = 9
So 909791-75-9 is a valid CAS Registry Number.

909791-75-9Upstream product

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909791-75-9Relevant academic research and scientific papers

An outstanding catalyst for asymmetric transfer hydrogenation in aqueous solution and formic acid/triethylamine

Matharu, Daljit S.,Morris, David J.,Clarkson, Guy J.,Wills, Martin

, p. 3232 - 3234 (2006)

A Rh/tetramethylcyclopentadienyl complex containing a tethered functionality has been demonstrated to give excellent results in the asymmetric transfer hydrogenation of ketones in both aqueous and formic acid/triethylamine media. The Royal Society of Chemistry 2006.

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