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3-(4-Bromo-phenylamino)-1,3-diphenyl-propan-1-ol is a complex organic compound with the molecular formula C19H18BrNO. It is characterized by the presence of a bromine atom attached to a phenyl ring, which is further connected to an amino group. This amino group is bonded to a propane-1-ol backbone, which also has two phenyl rings attached to it. The compound is known for its unique structure and potential applications in various chemical and pharmaceutical processes. Due to its specific functional groups and molecular arrangement, it may exhibit distinct chemical properties and reactivity, making it a subject of interest for researchers in the field of organic chemistry.

4566-59-0

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4566-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4566-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,6 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4566-59:
(6*4)+(5*5)+(4*6)+(3*6)+(2*5)+(1*9)=110
110 % 10 = 0
So 4566-59-0 is a valid CAS Registry Number.

4566-59-0Downstream Products

4566-59-0Relevant academic research and scientific papers

Direct introduction of nitrogen and oxygen functionality with spatial control using copper catalysis

Shaum, James B.,Fisher, David J.,Sroda, Miranda M.,Limon, Luis,De Alaniz, Javier Read

, p. 8748 - 8752 (2018)

Synthetic chemists have spent considerable effort optimizing the synthesis of nitrogen and oxygen containing compounds through a number of methods; however, direct introduction of N- and O-functionality remains challenging. Presented herein is a general method to allow for the simultaneous installation of N- and O-functionality to construct unexplored N-O heterocyclic and amino-alcohol scaffolds. This transformation uses earth abundant copper salts to facilitate the formation of a carbon-centered radical and subsequent carbon-nitrogen bond formation. The intermediate aminoxyl radical is terminated by an intramolecularly appended carbon-centered radical. We have exploited this methodology to also access amino-alcohols with a range of aliphatic and aromatic linkers.

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