22219-63-2

Usage

InChI:InChI=1/C15H14O4/c16-15(17)12-6-8-14(9-7-12)19-11-10-18-13-4-2-1-3-5-13/h1-9H,10-11H2,(H,16,17)

Upstream product

• 589-10-6 phenoxyethyl bromide 
• 24041-24-5 4-(2-phenoxy-ethoxy)-benzoic acid methyl ester 
• 122-99-6 2-Phenoxyethanol 
• 56442-09-2 ethyl 4-(2-phenoxyethoxy)benzoate 
• 25389-23-5 ethyl 4-(2-hydroxyethoxy)benzoate 
• 99-76-3 methyl 4-hydroxylbenzoate 

Downstream Products

• 127955-77-5 4-(2-phenoxy-ethoxy)-benzoyl chloride 

Relevant academic research and scientific papers

Synthesis of novel benzohydrazide and benzoic acid derivatives: Crystal Structure, Hirshfeld surface analysis and DFT computational studies

New series of benzohydrazide/benzoic acid derivatives were synthesized (4a-b and 5a-b) and subjected to solid-state characterization by NMR spectroscopic measurements. The molecular and crystal structures of 4a and 5a have also been examined by single-crystal X-ray crystallography were reveal that naphthalene frameworks are close to planarity. Besides, the dihedral angle between the mean plane of the naphthalene ring system and the phenyl ring is 2.26(7) and 78.87(8)° for 4a and 5a, respectively. The molecules are linked through N—H?O and C—H?O hydrogen bonds, forming chains parallel to the ab plane in benzohydrazide and O—H?O contacts in benzoic acid. The sheets are further stacked through C—H?π interactions resulting in the formation of a 3D supramolecular network. Hirshfeld surface analysis has also been performed to investigate intermolecular interactions in the solid-state; the most important contributions for the crystal packing are from H?H, C?H/H?C, and O?H/H?O interactions. Additionally, DFT calculations with the B3LYP/6-311G (d, p) level of the theory have been used to analyze the Mulliken atomic charges, molecular electrostatic potential map, and non-linear optical properties of the compounds were produced using the optimized structures. Moreover, the natural bond orbital analysis is conducted to explore the interactions among different orbital and lone pairs taking place within the compounds. The energy framework calculations suggest that the contacts formed between molecules are largely dispersive.

Benzimidazole inhibitors of hepatitis C virus NS5B polymerase: Identification of 2-[(4-diarylmethoxy)phenyl]-benzimidazole

A series of 1-cycloalkyl-2-phenyl-1H-benzimidazole-5-carboxylic acid derivatives was synthesized and evaluated for inhibitory activity against HCV NS5B RNA-dependent RNA polymerase (RdRp). A SAR study was performed and led to identify the 2-[(4-diarylmeth

PHENYL HYDROXAMIC ACIDS INCLUDING A HETERO-CONTAINING SUBSTITUENT

Phenyl hydroxamic acids are disclosed having the general formula or a pharmaceutically acceptable salt thereof, wherein X is NR, oxygen, sulfur, or a single bond, and Y is NR, oxygen, sulfur, or a single bond, where R can be hydrogen or lower alkyl, g can be 1 or 2, and with the proviso that at least one of X and Y is other than a single bond; Z is aryl, aralkyl or cycloalkyl; R1 is hydrogen, substituted or unsubstituted lower alkyl, cycloalkyl, lower alkenyl or aryl; R2 is hydrogen, lower alkyl, aroyl or acyl; m is 0 to 4 carbon atoms; and, n is 0 to 4 carbon atoms further providing that if one of X or Y is oxygen, the other of X or Y must be oxygen and further that when X and Y are oxygen Z cannot be aralalkyl. These new compounds have been found to be inhibitors or arachidonic acid 5-lipoxygenase and are therefore useful as antiallergy agents and antipsoriatics.