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(Z)-3-(4-bromophenyl)-3-(3-pyridyl)-2-propen-1-ol N-oxide is a complex organic compound with the molecular formula C15H12BrNO. It is characterized by a 2-propen-1-ol backbone, which is a type of alcohol with a double bond between the first and second carbon atoms. The molecule features a 4-bromophenyl group, which is a phenyl ring (a benzene ring) with a bromine atom attached at the 4th position, and a 3-pyridyl group, which is a pyridine ring with a nitrogen atom at the 3rd position. The N-oxide designation indicates that the nitrogen atom in the pyridine ring has an additional oxygen atom attached, forming a nitrogen oxide. (Z)-3-(4-bromophenyl)-3-(3-pyridyl)-2-propen-1-ol N-oxide is likely to be used in chemical research or as an intermediate in the synthesis of more complex molecules, given its unique structure and functional groups.

82589-75-1

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82589-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82589-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,8 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82589-75:
(7*8)+(6*2)+(5*5)+(4*8)+(3*9)+(2*7)+(1*5)=171
171 % 10 = 1
So 82589-75-1 is a valid CAS Registry Number.

82589-75-1Relevant academic research and scientific papers

Metabolites of the Pyridylallylamine Zimelidine Syntheses via α,β-Unsaturated Aldehydes with Conservation of Stereochemistry

Hoegberg, Thomas,Lundstroem, Jan

, p. 85 - 90 (2007/10/02)

Some tentative metabolites and metabolic intermediates of (Z)-3-(4-bromophenyl)-N,N-dimethyl-3-(3-pyridyl)allylamine (1, zimelidine) were synthesized. (Z)-3-(4-Bromophenyl)-3-(3-pyridyl)-2-propenal (8) and its N-oxide (15) were used in syntheses of N-methyl-hydroxylamines (17, 18), the pyridyl N-oxide of zimelidine (16) and a nitrone (19).The nitrone was also formed by oxidation of the allylic carbon of the corresponding N-methylhydroxylamine 17 with silver oxide.The compounds were diastereomerically pure and shown to possess the Z-configuration by means of UV and 1H NMR.

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