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(2E)-2-(4-bromophenyl)-3-pyridin-3-ylacrylic acid is a complex organic chemical compound characterized by a unique molecular structure. It is a conjugated molecule with a double bond (E configuration) between the 2- and 3-positions, featuring a 4-bromophenyl group attached to the 2-position and a pyridin-3-yl group at the 3-position. (2E)-2-(4-bromophenyl)-3-pyridin-3-ylacrylic acid belongs to the class of acrylic acids and exhibits properties associated with both phenyl and pyridine rings, as well as the presence of a bromine atom, which may influence its reactivity and potential applications in various chemical and pharmaceutical processes.

5847-76-7

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5847-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5847-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5847-76:
(6*5)+(5*8)+(4*4)+(3*7)+(2*7)+(1*6)=127
127 % 10 = 7
So 5847-76-7 is a valid CAS Registry Number.

5847-76-7Relevant academic research and scientific papers

LARGE CONDUCTANCE CALCIUM-ACTIVATED K CHANNEL OPENER

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Page/Page column 177, (2010/02/11)

The present invention provides a large conductance calcium-activated K channel opener comprising a compound of the formula (I): wherein R1 and R3 are each sulfonamide, carbamoyl, acyl, amino, and the like, m and n are each 0 to 2, R2 and R4 are each cyano, nitro, hydroxyl, an alkoxy, a halogen, or an alkyl, Ring A is benzene or a heterocyclic ring, Ring B is benzene, a heterocyclic ring, a cycloalkane etc, and Ring Q is pyrazole or isoxazole, or a pharmaceutically acceptable salt thereof as an active ingredient.

Effect of substituents on the 13C NMR chemical shifts of para-substituted α-phenyl-β-pyridylacrylic acids

Jovanovi?,Mi?i?-Vukovi?,Drmani?,?anadi

, p. 39 - 41 (2007/10/03)

The 13C NMR spectra of para-substituted α-phenylcinnamic and 3- and 4-pyridylacrylic acids, with a wide range of substituents effects, were determined in deuterated dimethylsulfoxide (DMSO-d6). The effect of substituents in both the α-phenyl and β-pyridine groups in these acids is investigated using linear free energy relationships and multiple regression analysis as applied to 13C NMR chemical shifts of the C(α) and C(β) of the ethylenic bond and the carboxylic group carbon. Dissection of the α-phenyl substituent effects into the inductive and resonance components, using the dual substituent parameter (DSP) method, points to a blend of inductive and resonance effects in the π-electronic system.

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