Category: 23351-09-9

Li, Shuhong published the artcileStudy on changes of volatile components in instant scallop before and after sterilization, Category: alcohols-buliding-blocks, the publication is Shipin Gongye Keji (2012), 33(4), 117-121, database is CAplus.

The influence of sterilization on flavor components in instant scallop was investigated. Gas chromatog.-mass spectrometry (GC-MS) combined with technique of headspace solid phase micro-extraction (HS-SPME) was used to analyze flavor components in instant scallop before and after sterilization. The results showed that 117 flavor components in scallop before sterilization and 119 ones in scallop after sterilization, resp. In the instant scallop before sterilization, the content of alcs., aldehydes, esters, ketones, acids, aromatic series, furans, phenols, hydrocarbon and others content was 3.21%, 4.78%, 2.06%, 0.47%, 0.25%, 8.38%, 0.03%, 0.72%, 32.58% and 47.52%, the number was 7, 9, 9, 4, 2, 22, 1, 1, 33 and 29, resp. In the instant scallop after sterilization, the content of alcs., aldehydes, esters, ketones, acids, aromatic series, furans, phenols, hydrocarbon and others content was 2.85%, 4.48%, 11.54%, 0.90%, 0.49%, 7.81%, 0.86%, 0.55%, 28.20% and 42.32%, the number was 9, 11, 11, 6, 5, 15, 5, 3, 32 and 22, resp., 67 ingredients species were the same in before and after sterilization scallop. The contents of aroma components of instant scallops after sterilization esters and furans were significantly more than that before sterilization. Thus sterilization process on the aroma components of instant scallop had a role in the retention and aroma, making instant scallop seafood was more dense fragrance, aroma coordination.

Shipin Gongye Keji 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, Category: alcohols-buliding-blocks.

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

Polat, Merve Pamukcu published the artcileMetallophthalocyanines bearing four 3-(pyrrol-1-yl)phenoxy units as photosensitizer for dye-sensitized solar cells, Quality Control of 23351-09-9, the publication is Dyes and Pigments (2018), 267-275, database is CAplus.

In this article, the synthesis of non-peripheral metallophthalocyanines (cobalt, zinc, and manganese) bearing four 3-(pyrrol-1-yl)phenoxy units was reported. The new compounds have been characterized using UV-Vis, FT-IR, ¹H NMR, and mass spectroscopic data. Aggregation behaviors of phthalocyanines were investigated in concentrations ranging from 14 × 10^-6 to 2 × 10^-6 M. Electrochem. measurements gave well illustrated redox activities of MnClPc and CoPc. Electrochem. and spectroelectrochem. studies showed that MnClPc gives two metal-based reduction processes in addition to the one ring-based reduction and one ring-based oxidation process. Distinct color differences between the electrogenerated MnClPc species were observed during in situ spectroelectrochem. measurements. The potential of these compounds as photosensitizers and dependence of the photovoltaic performance on the thickness of photoanode layer were investigated. For this purpose, DSSC devices were fabricated with the structure of FTO/TiO₂:4-6/Electrolyte/Pt/FTO and characterized under AM 1.5 illuminations. By using 6 as dye a photovoltaic conversion efficiency of 2.44% with short circuit c.d. of 7.17 mA cm^-2 and open circuit voltage of 0.68 V was observed

Dyes and Pigments 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, Quality Control of 23351-09-9.

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

Diaw, A. K. D. published the artcileSynthetic routes, characterization, electrochemical and spectral properties of p-substituted N-phenylpyrroles, HPLC of Formula: 23351-09-9, the publication is ARKIVOC (Gainesville, FL, United States) (2008), 122-144, database is CAplus.

A series of p-substituted N-phenylpyrroles, including 4-(1H-pyrrol-1-yl)phenol, 1-(4-methoxyphenyl)-1H-pyrrole, 1,1′-benzene-1,4-diylbis(1H-pyrrole), 1,1′-biphenyl-4,4′-diylbis(1H-pyrrole), and 1-(4-bromophenyl)-1H-pyrrole (I), was prepared by means of a modified Clauson-Kaas method. Two new sym. and asym. end-capped pyrrole thiophenes, namely 1-[4-(thiophen-2-yl)phenyl]-1H-pyrrole and 1,1′-(bithiophen-5,5”-diyldibenzene-4,1-diyl)bis(1H-pyrrole), were synthesized by using I as a building block and the Stille method as cross-coupling reaction. For both methods, the chem. yields ranged from 36 to 81% and the desired products were characterized by ¹H and ¹³C NMR, IR, and mass spectrometry. Electrochem. properties and UV-visible absorption spectra were also investigated in order to evaluate the substituent electron-donor effects on the physicochem. parameters.

ARKIVOC (Gainesville, FL, United States) 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, HPLC of Formula: 23351-09-9.

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

Wang, Xuewei published the artcileYnamide-Mediated Intermolecular Esterification, Recommanded Product: 4-(1H-Pyrrol-1-yl)phenol, the publication is Journal of Organic Chemistry (2020), 85(9), 6188-6194, database is CAplus and MEDLINE.

An ynamide-mediated one-pot, two-step intermol. esterification via the condensation of carboxylic acids with nucleophilic hydroxyl species is reported. A broad substrate scope with respect to carboxylic acids, alcs., and phenols is observed The α-acyloxyenamide intermediates formed by the addition of carboxylic acids to ynamides proved to be effective acylating reagents for the esterification of alc. and phenol derivatives with the assistance of base catalysis. Notably, the racemization of the α-chiral center of carboxylic acids can be avoided.

Journal of Organic 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 C18H35NO, Recommanded Product: 4-(1H-Pyrrol-1-yl)phenol.

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

Liu, Xiaojie published the artcileNi-Catalyzed Deoxygenative Borylation of Phenols Via O-Phenyl-uronium Activation, Formula: C10H9NO, the publication is ACS Catalysis (2022), 12(15), 8904-8910, database is CAplus.

Herein, we report an efficient method for the Ni-catalyzed deoxygenative borylation of unprotected phenols and also demonstrate that this Ni-catalyzed phenolic C(sp²)-O transformation is applicable to the Suzuki-Miyaura-type and Heck-type cross-couplings of phenols. Investigations on the reaction intermediate have revealed that the achievement of general, mild deoxygenative cross-coupling reactions of phenols is ascribed to the conversion of phenols into the unusual O-phenyl-uroniums that feature active phenolic C(sp²)-O bonds. The Ni-complex intermediate resulting from an oxidative addition of a phenolic C(sp²)-O bond to monophosphine-supported Ni(0) catalyst was characterized and confirmed to be (PCy₃)₂Ni(Ar)(F) complex, offering exptl. evidence for the generally proposed C(sp²)-O oxidative addition step.

ACS Catalysis 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, Formula: C10H9NO.

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

Hong, Fengying published the artcileN-terminal strategy (N1-N4) toward high performance liquid crystal materials, Application In Synthesis of 23351-09-9, the publication is Tetrahedron (2016), 72(10), 1285-1292, database is CAplus.

Liquid crystal materials have a variety of applications in many fields such as display techniques as well as photonics and optics. However, only few design principles have been disclosed on liquid crystal materials with different N-heterocycles as the terminal groups, which hinder the development of the heterocyclic liquid crystals. Here, a strategy of mol. design for N-heterocyclic liquid crystal materials is reported. On the basis of this strategy, a series of convenient N-heterocycles such as pyrrole, pyrazole, imidazole, 1,2,3-triazole, 1,2,4-triazole, 1,2,3,4-tetrazole were applied to synthesize the novel liquid crystals. Most of them have proved to exhibit good mesomorphic behaviors which make them excellent components in the mixture of the LCDs materials. The simple attachment of N-heterocyclic units to the liquid crystal mols. through a mild reaction condition will provide a good prospect for the design of N-heterocyclic liquid crystals.

Tetrahedron 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 In Synthesis of 23351-09-9.

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

Liu, Lili published the artcileCopper-catalysed N-arylation of pyrrole with aryl iodides under ligand-free conditions, COA of Formula: C10H9NO, the publication is Journal of Chemical Research (2014), 38(3), 180-182, database is CAplus.

A simple, inexpensive and ligand-free copper-catalyzed N-arylation of nitrogen containing heterocycles such as pyrrole, imidazole, indole, and benzimidazole with aryl iodides has been developed, giving N-arylated products in moderate to excellent yields. The catalyst loading is relative low (5 mol%) and the catalyst system was stable in air.

Journal of Chemical Research 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, COA of Formula: C10H9NO.

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

Kang, Iou-Jiun published the artcileDesign, synthesis, and anti-HCV activity of thiourea compounds, Formula: C10H9NO, the publication is Bioorganic & Medicinal Chemistry Letters (2009), 19(7), 1950-1955, database is CAplus and MEDLINE.

A series of thiourea derivatives, e.g., I, were synthesized and their antiviral activity was evaluated in a cell-based HCV subgenomic replicon assay. SAR studies revealed that the chain length and the position of the alkyl linker largely influenced the in vitro anti-HCV activity of this class of potent antiviral agents. Among this series of synthesized compounds, the thiourea derivative with a six-carbon alkyl linker at the meta-position of the central Ph ring was identified as the most potent anti-HCV inhibitor (EC₅₀ = 0.047 μM) with a selectivity index of 596.

Bioorganic & Medicinal Chemistry Letters 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, Formula: C10H9NO.

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

Su, Chang published the artcileSyntheses and properties of pyrrole derivative as a cathode material for Li-ion batteries, Recommanded Product: 4-(1H-Pyrrol-1-yl)phenol, the publication is Applied Mechanics and Materials (2012), 731-735, database is CAplus.

A copolymer of 4-(1H-pyrrol-1-yl)phenol (PLPY) and pyrrole (P(PLPY-co-Py))was synthesized. And the chem. structure and battery performance of the prepared materials were characterized comparably by 1H NMR, FT-IR spectra and galvanostatic charge-discharge testing using simulant lithium ion half-cell method, resp. The results shows that the introduction of the phenol group to the pyrrole as a rigid side chain could prevent the polymer from agglomeration and optimize the particle morphol. of the resulting polymers, all of which made it demonstrate a significantly improved specific capacity (73.9 mAh·g^-1) compared with PPy (21.4 mAh·g^-1).

Applied Mechanics 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 C8H10BNO3, Recommanded Product: 4-(1H-Pyrrol-1-yl)phenol.

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

Su, Chang published the artcileSynthesis of a novel ferrocene-contained polypyrrole derivative and its performance as a cathode material for Li-ion batteries, Quality Control of 23351-09-9, the publication is Electrochimica Acta (2013), 302-307, database is CAplus.

A novel ferrocene-contained pyrrole, 4-(1H-pyrrol-1-yl)-Ph-ferrocenecarboxylate (FcPy) was synthesized by esterification of 4-(1H-pyrrol-1-yl)-phenol (PLPY) and ferrocenecarboxylic acid. Then the homopolymer of FcPy (PFcPy), copolymer of FcPy and pyrrole (P(FcPy-co-Py)), polypyrrole (PPy) were prepared by chem. oxidative polymerization And the structure, morphol., electrochem. properties of prepared polymers were characterized by FTIR spectroscopy, SEM, cyclic voltammograms (CV) and electrochem. impedance spectra (EIS), resp. Also, the charge/discharge properties of the prepared polymers were studied by galvanostatic charge-discharge testing. The introduction of ferrocene to polypyrrole obviously improved the specific capacity of PPy cathode and gave a well-defined plateau at the potential rang of ∼3.5 V. Under the authors’ exptl. conditions, the discharge capacity of undoped PPy-based electrodes only presented 16.5 mAh g^-1 at 20 mA g^-1 between 2.5 and 4.2 V, while PFcPy-based electrodes exhibited an initial discharge capacity of up to 43.2 mAh g^-1. Specially, the P(FcPy-co-Py)-based electrodes even showed a discharge capacity of 68.1 mAh g^-1 and the improved discharge platform, which were ascribed to the resonance doping effect of pendant group, the advanced electrochem. nature of ferrocene moiety and the loose morphol. of copolymer.

Electrochimica Acta 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 C7H7BN2O2, Quality Control of 23351-09-9.

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