Results 31 to 40 of about 2,566,479 (206)

2-(4-Bromobenzenesulfonamido)-2-phenylacetic acid monohydrate

Acta Crystallographica Section E, 2009
In the title compound, C14H12BrNO4S·H2O, the phenyl and benzene rings are inclined at a dihedral angle of 39.5 (5)°. The crystal packing is stabilized by N—H...O, C—H...O and O—H...O hydrogen ...
Muhammad Nadeem Arshad, Islam Ullah Khan, Mehmet Akkurt, Muhammad Shafiq   +3 more
doaj   +1 more source

Crystallographic and spectroscopic characterization of (R)-O-acetylmandelic acid

Acta Crystallographica Section E: Crystallographic Communications, 2016
The title compound [systematic name: (R)-(−)-2-acetoxy-2-phenylacetic acid], C10H10O4, is a resolved chiral ester derivative of mandelic acid. The compound contains an acetate group and a carboxylic acid group, which engage in intermolecular hydrogen ...
Cady Cirbes, Joseph M. Tanski
doaj   +1 more source

A Convenient Preparation 2,6-Dimethoxy phenylacetic Acid

, 1967
A Convenient Preparation 2,6-Dimethoxy phenylacetic ...
K. S. Nargund, S. N. Kulkarni, A. R. lnamdar   +2 more
core   +1 more source

Phenylacetic Acid (3S,6S)-6-Acetoxy-8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl Ester

Molbank, 2003
n ...
Yang Lu, Yin-Yao Niu
doaj   +1 more source

Acryloyloxy and methacryloyloxy derivatives of phenylacetic acid and their polymers

, 1987
2-Methacryloyloxy-2-phenylacetic acid (I), 2-acryloyloxy-2-phenylacetic acid (II), 4-methacryloyloxyphenylacetic acid (III), and 4-acryloyloxyphenylacetic acid (IV), ethyl 4-methacryloyloxyphenylacetate (V) and ethyl 4-acryloyloxyphenylacetate (VI) were ...
Milan Bezděk, Vladimír Kubánek, František Hrabák, Jan Lokaj, Hana Pivcová   +4 more
core   +1 more source

Biotransformation and Production from Hansenula Anomala to Natural Ethyl Phenylacetate

MATEC Web of Conferences, 2015
Ethyl phenylacetate can be widely applied in many industries, such as food, medicines, cosmetics and medicinal herbs. At the moment, the production of natural ethyl phenylacetate is very limited. However, the biotransformation production of natural ethyl
Tian Xun, Wang Jingwen, Li Qianqian, Guan Shimin, Cai Baoguo, Rong Shaofeng   +5 more
doaj   +1 more source

Synthesis, Crystal Structure and Catalytic Activity of a Novel Ba(II) Complex with Pyridine-2-Carboxaldehyde-2-Phenylacetic Acid Hydrazone Ligand

Crystals, 2017
A novel Ba(II) complex, [BaL2Cl2] (1) (L = pyridine-2-carboxaldehyde-2-phenylacetic acid hydrazone), has been synthesized using BaCl2, pyridine-2-carboxaldehyde and 2-phenylacetohydrazide as raw materials.
Li-Hua Wang, Xi-Shi Tai, Li-Li Liu, Peng-Fei Li   +3 more
doaj   +1 more source

The Bacteriostatic Activity of 2-Phenylethanol Derivatives Correlates with Membrane Binding Affinity

Membranes, 2021
The hydrophobic tails of aliphatic primary alcohols do insert into the hydrophobic core of a lipid bilayer. Thereby, they disrupt hydrophobic interactions between the lipid molecules, resulting in a decreased lipid order, i.e., an increased membrane ...
Isabel S. Kleinwächter, Stefanie Pannwitt, Alessia Centi, Nadja Hellmann, Eckhard Thines, Tristan Bereau, Dirk Schneider   +6 more
doaj   +1 more source

AS‐TLC‐Based High‐Throughput Screening Integrated with CuAAC Optimization Strategy Facilitates the Rapid Discovery of YTHDC1 Inhibitor

Advanced Science, EarlyView.
We developed Affinity Selection Thin‐Layer Chromatography (AS‐TLC) as a method for high‐throughput screening (HTS) of compound mixtures. Furthermore, we integrated activity assays with AS‐TLC and identified a YTH domain‐containing protein 1 (YTHDC1) inhibitor. Building on this hit, we applied copper(I)‐catalyzed azide–alkyne cycloaddition (CuAAC) click
Mingchen Wang, Shuiping Fu, Ye Xu, Jia Gao, Jiwei Ren, Xu Yang, Hesong Xu, Ge Sun, Yanjie Li, Yanlin Wang, Lu Jin, Peijuan Chen, Ying Xu, Jianhao Li, Hua Lin, Chujiao Hu, Kaixian Chen, Huan Xiong, Cheng Luo, Shijie Chen   +19 more
wiley   +1 more source

Crystallization‐Induced Emission Enhancements of Hybrid Butenolide‐Diphenylethenes

Chemistry – A European Journal, EarlyView.
Hybrid butenolide‐diphenylethene fluorophores show crystallization‐induced emission enhancement (CIEE), with substituents tuning solid‐state quantum yields up to 50%. One derivative, BuCM, displays dual‐state emissions (DSE), making this compact scaffold a promising platform for CIEE/DSE‐active fluorophores.
Sujlesh Sharma, Tuong Anh To, Ruoming Tian, Thanh Vinh Nguyen   +3 more
wiley   +1 more source