Category: 23351-09-9

Soganci, Tugba published the artcileFerrocenyldithiophosphonate Containing Conducting Polymers and Theirs Electrochromic Application, Formula: C10H9NO, the publication is Journal of Inorganic and Organometallic Polymers and Materials (2015), 25(5), 1011-1018, database is CAplus.

In this study, a new ferrocenyldithiophosphonate functionalized; [O-1-(4-phenyl)-1H-pyrrole ferrocenyldithiophosphonate (TPFc)] monomer and its conductive copolymers with pyrrole and 4-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)butane-1-amine were synthesized, characterized and their electrochromic properties were investigated. The spectroelectrochem. analyses demonstrated that the copolymer films reveal a reversible cycling with distinctive color changes in their reduced/oxidized forms. For the copolymer films P(TPFc-co-Py)/DCM, P(TPFc-co-Py)/CH3CN and P(TPFc-co-TPA)/DCM, the maximum optical contrasts (ΔT %) were measured as 28, 12 and 27% at 800, 900 and 900 nm, resp. Spectroelectrochem. anal. also revealed that all copolymers prepared with TPFc have lower band gaps compared to those of corresponding polymers.

Journal of Inorganic and Organometallic Polymers and Materials published new progress about 23351-09-9. 23351-09-9 belongs to alcohols-buliding-blocks, auxiliary class Pyrrole,Benzene,Alcohol, name is 4-(1H-Pyrrol-1-yl)phenol, and the molecular formula is C4H6O3, Formula: C10H9NO.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Zhao, Fengqian published the artcileRadical Carbonylation under Low CO Pressure: Synthesis of Esters from Activated Alkylamines at Transition Metal-Free Conditions, Product Details of C10H9NO, the publication is Chinese Journal of Chemistry (2021), 39(4), 927-932, database is CAplus.

High CO pressure (> 40 bar) is usually needed in radical carbonylation reactions in the absence of metal catalyst. In this communication, a transition-metal-free radical carbonylation of activated alkylamines with phenols and alcs. under low CO pressure (1-6 bar) was developed. Various esters were obtained in moderate to excellent yields under simple reaction conditions with good functional group compatibility.

Chinese Journal of Chemistry published new progress about 23351-09-9. 23351-09-9 belongs to alcohols-buliding-blocks, auxiliary class Pyrrole,Benzene,Alcohol, name is 4-(1H-Pyrrol-1-yl)phenol, and the molecular formula is C39H35N5O8, Product Details of C10H9NO.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Kirkland, Thomas A. published the artcileSynthesis of glutamic acid analogs as potent inhibitors of leukotriene A₄ hydrolase, Application of 4-(1H-Pyrrol-1-yl)phenol, the publication is Bioorganic & Medicinal Chemistry (2008), 16(9), 4963-4983, database is CAplus and MEDLINE.

Leukotriene B₄ (LTB₄) is a potent pro-inflammatory mediator that has been implicated in the pathogenesis of multiple diseases, including psoriasis, inflammatory bowel disease, multiple sclerosis and asthma. As a method to decrease the level of LTB₄ and possibly identify novel treatments, inhibitors of the LTB₄ biosynthetic enzyme, leukotriene A₄ hydrolase (LTA₄-h), have been explored. Here, the authors describe the discovery of a potent inhibitor of LTA₄-h, arylamide of glutamic acid derivative I, starting from Boc-Glu[NHC₆H₄(OCH₂Ph)-4]-OH. Analogs of I are then described, focusing on compounds that are both active and stable in whole blood. This effort culminated in the identification of amino alc. II and amino ester III which meet these criteria.

Bioorganic & Medicinal Chemistry published new progress about 23351-09-9. 23351-09-9 belongs to alcohols-buliding-blocks, auxiliary class Pyrrole,Benzene,Alcohol, name is 4-(1H-Pyrrol-1-yl)phenol, and the molecular formula is C10H9NO, Application of 4-(1H-Pyrrol-1-yl)phenol.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts