109799-62-4

Upstream product

• 643-43-6 (2,4-dinitro-phenyl)-acetic acid 
• 79-37-8 oxalyl dichloride 

Downstream Products

• 52887-14-6 (2,4-dinitro-phenyl)-acetic acid-(4-dimethylamino-anilide) 
• 2200-86-4 1-(2,4-dinitrophenyl)propan-2-one 
• 100130-65-2 (2,4-dinitro-phenyl)-acetic acid amide 
• 349419-18-7 2-(2,4-dinitro-phenyl)-N-phenyl-acetamide 
• 33589-96-7 (2,4-dinitro-phenyl)-acetic acid-(N'-phenyl-hydrazide) 
• 58665-14-8 p-[1-benzoyl-1'-(2,4-dinitrophenyl)methane] 
• 33589-94-5 Benzoic acid N'-[2-(2,4-dinitro-phenyl)-acetyl]-N'-phenyl-hydrazide 
• 33250-96-3 1-Chlor-2-oxo-3-(2,4-dinitrophenyl)propan 
• 31984-11-9 1-bromo-3-(2,4-dinitro-phenyl)-acetone 
• 540750-27-4 (6-nitro-benz[d]isoxazol-3-yl)-phenyl ketone 
• 1382271-05-7 N-(2,5-dimethoxyphenyl)-2-(2,4-dinitrophenyl)-N-phenylacetamide 
• 349431-27-2 C₁₀H₁₁N₃O₅ 
• 1354724-84-7 2-(2,4-dinitrophenyl)-N,N-dimethylethanethioamide 
• 1354724-74-5 (R)-N-(1-(5-(dimethylamino)-4-(2,4-dinitrophenyl)thiophen-2-yl)heptyl)-4-methylbenzenesulfonamide 

Relevant academic research and scientific papers

pH-MODULATED QUENCHERS OF FLUORESCENCE

The present disclosure relates to a compound of formula (I) or a salt thereof, wherein variable A, B, and X are as defined herein. The disclosure also relates to covalent conjugates of formula (II). The disclosure further relates to the use of the compoun

Optically active thiophenes via an organocatalytic one-pot methodology

A general methodology for the synthesis of trisubstituted, optically active thiophenes by an organocatalytic one-pot reaction cascade is presented. The target products are synthesized in good yields (up to 92%) and with excellent enantioselectivities (up to 98% ee). Importantly, based on practical and easily available starting materials, the presented methodology can be conducted under mild reaction conditions. To further elucidate the generality, the synthesis of optically active thienoindoles, as well as selenophenes, is also demonstrated.

Syntheses of unsymmetrically N,N′-bis (substituted)-4,13-diaza-18-crown-6-ether derivatives as a new electron donor-spacer-acceptor triad

A simple and general synthetic strategy potentially applicable for the preparation of a wide variety of unsymmetrically N,N′-bis(substituted)-4, 13-diaza-18-crown-6-ether derivatives was reported.