69642-00-8

Upstream product

• 612-22-6 2-nitro(ethylbenzene) 
• 80379-10-8 1-(2-nitrophenyl)ethan-1-ol 

Downstream Products

• 688044-24-8 2-({6-chloro-7-[1-(2-nitro-phenyl)-ethoxy]-2-oxo-2H-chromene-3-carbonyl}-amino)-pentanedioic acid dimethyl ester 
• 688044-40-8 {tert-butoxycarbonylmethyl-[4-({6-chloro-7-[1-(2-nitro-phenyl)-ethoxy]-2-oxo-2H-chromene-3-carbonyl}-amino)-cyclohexyl]-amino}-acetic acid tert-butyl ester 
• 85062-52-8 3-(4-Methoxy-benzyl)-4-methyl-3,4-dihydro-quinazolin-2-ylamine; hydrobromide 
• 85062-71-1 4-(4-Methoxy-benzyl)-5-methyl-4,5-dihydro-imidazo[1,2-a]quinazolin-2-one; hydrochloride 
• 1620751-79-2 (±)-N-{1-[1-(2-nitrophenyl)ethoxy]-2,2,6,6-tetramethylpiperidin-4-yl}benzamide 
• 1384516-79-3 1-nitro-2-(1-phenoxyethyl)benzene 
• 1384516-72-6 2-[1-(2-nitrophenyl)ethoxy]benzaldehyde 
• 1384575-72-7 C₂₉H₃₂BN₃O₅ 
• 1384575-44-3 (O₂NC₆H₄CH(CH₃)OC₆H₄C(C₄HN(CH₃)2)2)BF₂ 
• 1384516-77-1 C₃₁H₃₀N₃O₄⁽¹⁺⁾*Cl^(1-) 
• 1402719-11-2 1-(2-nitrophenyl) ethyl 6-hydroxyhexanoate 
• 1402719-19-0 C₂₃H₃₈N₃O₄PS 
• 1402719-18-9 C₂₃H₃₆N₃O₆P 
• 1402719-12-3 6-[1-(2-nitrophenyl)ethylthio]hexan-1-ol 

Relevant academic research and scientific papers

SNAP-tag-reactive lipid anchors enable targeted and spatiotemporally controlled localization of proteins to phospholipid membranes

The natural mechanisms that direct proteins to membranes are typically complex, requiring multiple steps and accessory components. It would be advantageous to develop simplified methods to direct proteins of interest to phospholipid membranes in a single

MOLECULES HAVING CERTAIN PESTICIDAL UTILITIES, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES RELATED THERETO

This disclosure relates to compounds having pesticidal utility against pests in phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such compounds and intermediates used in such processes, compositions containing such compounds, and processes of using such compounds against such pests. These compounds/molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses compounds having the following formula (Formula One and/or Formula One-A).

A Light-Controllable Chemical Modulation of m6A RNA Methylation

Bioactive small molecules with photo-removable protecting groups have provided spatial and temporal control of corresponding biological effects. We present the design, synthesis, computational and experimental evaluation of the first photo-activatable sma

Intramolecular Pd-catalyzed reductive amination of enolizable sp3-C-H bonds

A palladium-catalyzed reductive cyclization of nitroarenes has been designed to construct sp3-C-NHAr bonds from sp3-C-H bonds by using an enolizable nucleophile to intercept a nitrosoarene intermediate. Exposure of ortho-substituted nitroarenes to 5 mol ?% of Pd(OAc)2 and 10 mol ?% of phenanthroline under 2 atm of CO constructs partially saturated 5-, 6-, or 7-membered N-heterocycles using α-pyridyl carboxylates, malonates, 1,3-dimethylbarbituric acid, 1,3-diones, or difurans as the nucleophile.

Fluorescence imaging mitochondrial copper(II) via photocontrollable fluorogenic probe in live cells

Monitoring mitochondrial derived copper(II) in live cells is highly demanded, but accurately detecting is unmet due to the interference with cytoplasmic copper(II). Herein, we have reported the design, synthesis and characterization of photocontrollable f

Photolabile protecting groups for nitroxide spin labels

Nitroxide spin labels can be protected against critical conditions of DNA/RNA or peptide synthesis by reduction and alkylation with light-sensitive groups such as nitrobenzyl- or aminocoumarins. High chemical stability qualifies tetraethylisoindoline 5 an

Photocaging strategy for functionalisation of oligonucleotides and its applications for oligonucleotide labelling and cyclisation

We have used a photocaging strategy to develop novel phosphoramidites and expand the repertoire of protecting groups for modification of oligonucleotides by solid-phase synthesis. We synthesised five photolabile phosphoramidites and four new photolabile c

2-alkyl sulfonyl-1,4-diaminobenzenes, processes for their production and oxidation hair dyeing compositions containing the same

Novel 2-alkyl sulfonyl ethyl-1,4-diaminobenzenes of formula 1 STR1 wherein R denotes CH3 or C2 H5 and the salts thereof, a process for making the compositions of formula I as well as compositions for the oxidative dyeing o