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55591-48-5

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55591-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55591-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,9 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55591-48:
(7*5)+(6*5)+(5*5)+(4*9)+(3*1)+(2*4)+(1*8)=145
145 % 10 = 5
So 55591-48-5 is a valid CAS Registry Number.

55591-48-5Relevant academic research and scientific papers

Oligo(U-terpyridines) and their ruthenium(II) complexes: Synthesis and structural properties

Winter, Andreas,Hummel, Johanna,Risch, Nikolaus

, p. 4862 - 4871 (2006)

A highly efficient domino reaction starting from tetrahydroquinolinone and a series of bisiminium salts provides the corresponding bis(U-terpyridines). These ligands have been treated with [(tpy)RuCl3] to afford novel dinuclear complexes [(tpy)

Rediscovering aminal chemistry: Copper(ii) catalysed formation under mild conditions

Afonso, Carlos A. M.,António, Jo?o P. M.,Gomes, Rafael F. A.,Mendon?a, Ricardo,Pereira, Juliana G.

supporting information, p. 7484 - 7490 (2020/11/18)

Aminals, the N,N analogues of acetals, have been thoroughly explored in organic chemistry, with a particular focus on heteroaromatic aldehyde lithiation. Nevertheless, the existing methodologies for their formation typically employ harsh conditions limiting their usefulness. In this work, we present an efficient and mild methodology for the preparation of aminals from aromatic aldehydes, including furanic platforms. These mild conditions allowed ease of access to a plethora of aminals and as such we set out to explore previously unaccessible potential applications. By studying the stability of various aminals, we were able to develop a simple aldehyde protecting group based on a commercial diamine which is deprotected under mind conditions. We developed a protocol for the scavenging of genotoxic aldehydes by taking advantage of our methodology and a diamine resin, as well as early studies on the development of a stimuli-responsive release system using a salycil aldehyde derived aminal. This journal is

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