711-41-1

Usage

Appearance

Yellow crystalline solid

Usage

a. Production of dyes
b. Reagent for amino acid analysis
c. Production of pharmaceuticals

Classification

Nitroaromatic compound

Nitro groups

Contains two NO2 groups attached to an aromatic ring

Toxicity

Toxic if inhaled, ingested, or absorbed through the skin

Carcinogenicity

Potential human carcinogen

Handling and disposal

Requires careful handling and disposal due to its toxicity and carcinogenic potential

Upstream product

• 106-42-3 para-xylene 
• 7697-37-2 nitric acid 
• 89-58-7 mononitro-p-xylene 

Downstream Products

• 35975-12-3 3,6-dimethylbenzene-1,2-diamine 
• 121187-64-2 2,3-dinitroterephthalic acid 
• 69272-51-1 4,7-dimethyl-1,3-dihydro-benzoimidazol-2-one 
• 69272-53-3 2-Chlor-4,7-dimethyl-benzimidazol 
• 1375277-78-3 (S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(3-ethyl-4,7-dimethyl-2-oxo-2,3-dihydrobenzo[d]imidazol-1-yl)acetamido)-N-methyl-3-phenylpropanamide 
• 66-71-7 1,10-Phenanthroline 
• 484-11-7 2.9-dimethyl-1,10-phenanthroline 
• 773883-32-2 2,9-di(pyridin-2-yl)-1,10-phenanthroline 
• 113397-69-6 (1E,1'E)-2,2'-(2,3-dinitro-1,4-phenylene)bis(N,N-dimethylethen-1-amine) 
• 74157-74-7 1,4-dimethyl-2-nitro-3-(phenylsulfonyl)benzene 
• 74157-75-8 C₁₇H₁₉NO₂S 
• 74157-73-6 1.4-Dimethyl-2-nitro-3-phenylthiobenzol 
• 90437-65-3 2-Nitro-3,6,N-trimethyl-anilin 
• 6370-24-7 2-amino-3,6-dimethyl-benzenesulfonic acid 

Relevant academic research and scientific papers

Nitration of deactivated aromatic compounds via mechanochemical reaction

A variety of deactivated arenes were nitrated to their corresponding nitro derivatives in excellent yields under high-speed ball milling condition using Fe(NO3)3·9H2O/P2O5 as nitrating reagent. A radical involved mechanism was proposed for this facial, eco-friendly, safe, and effective nitration reaction.

Mechanism-Inspired Design of Bifunctional Catalysts for the Alternating Ring-Opening Copolymerization of Epoxides and Cyclic Anhydrides

Advances in catalysis have enabled the ring-opening copolymerization of epoxides and cyclic anhydrides to afford structurally and functionally diverse polyesters with controlled molecular weights and dispersities. However, the most common systems employ b

Asymmetric Hydrogenation of 3,5-Bistrifluoromethyl Acetophenone in Pilot Scale with Industrially Viable Ru/Diphosphine-Benzimidazole Complexes

A novel efficient asymmetric hydrogenation (AH) process was developed for the preparation of (R)-1-(3,5-bis(trifluoromethyl)phenyl)ethanol (3), using a catalyst Ru/(4R,5R)-(+)-4,5-bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxoane-(R,R-Diop)-2R-(α-met

NOVEL ANTIVIRAL COMPOUNDS

The present invention relates to a compound of formula I: or a pharmaceutically acceptable salt thereof, wherein the symbols are as defined in the specification; a pharmaceutical composition comprising the same, a method for treating or preventing a viral infection such as HIV using the same.

Synthesis and characterization of Nitro-p-xylenes

In this paper we elected to nitrate p-xylene because this compound has only one mononitro- and trinitro- isomer. Trinitro-p-xylene was used as a starting material for the synthesis of other compounds in subsequent work. The mononitration of p-xylene can be easily carried out at 30°C. Nitro-p-xylene is easily nitrated to dinitro-p-xylene at a temperature of 80°C. The trinitro-p-xylene can be obtained at 120°C. Single crystals of 2,3-dinitro-p-xylene and 2,3,5-trinitro-p-xylene were grown using the slow cooling method and we report the X-ray structure of the former. The thermal decomposition of the compounds was studied using differential scanning calorimetry (DSC) and thermogravimetry-derivative thermogravimetry (TG-DTG) techniques and FT-IR. The target compounds were also characterized by 1H-NMR, 13C-NMR and MS.