881-67-4

Basic information

• Product Name: Benzene, 1-(dimethoxymethyl)-4-nitro-
• CAS NO: 881-67-4
• Molecular Formula: C9H11NO4
• Molecular Weight: 197.191
• Mol File: 881-67-4.mol
• Article Data: 74

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(dimethoxymethyl)-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(dimethoxymethyl)-4-nitro-(881-67-4)
• EPA Substance Registry System: Benzene, 1-(dimethoxymethyl)-4-nitro-(881-67-4)

Safety Data

• Hazardous Substances Data: 881-67-4(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 555-16-8 4-nitrobenzaldehdye 
• 122-04-3 4-nitro-benzoyl chloride 
• 99-99-0 1-methyl-4-nitrobenzene 
• 89712-45-8 N,N-dimethylformamide dimethyl sulfate adduct 
• 149-73-5 trimethyl orthoformate 
• 24588-74-7 4-nitrophenyl-1,3-dithiane 
• 7647-01-0 hydrogenchloride 
• 2403-62-5 p-nitrobenzaldehyde diethyl acetal 
• 1129-37-9 4-nitrobenzaldehyde oxime 
• 628300-14-1 2,4-dichloro-3-(1,3-propylenedithio-methylene)-penta-1,4-diene 
• 39184-67-3 3-chloro-3-(p-nitrophenyl)diazirine 
• 110-89-4 piperidine 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 619-50-1 4-nitrobenzoic acid methyl ester 
• 3516-76-5 4-phenylazobenzaldehyde 
• 56377-72-1 (α-Chlor-4-nitrobenzyl)methylether 
• 93136-94-8 Methoxy-tert.-butylperoxy-<4-nitro-phenyl>-methan 
• 64533-24-0 1-(Methanesulfonyl-methoxy-methyl)-4-nitro-benzene 
• 64533-23-9 C₁₅H₁₅NO₅S 
• 64533-22-8 C₁₄H₁₂ClNO₅S 
• 64533-21-7 1-(Benzenesulfonyl-methoxy-methyl)-4-nitro-benzene 
• 91256-90-5 1-((1S,2S)-2-Bromo-1,3,3-trimethoxy-propyl)-4-nitro-benzene 
• 91256-90-5 1-((1S,2R)-2-Bromo-1,3,3-trimethoxy-propyl)-4-nitro-benzene 
• 92594-60-0 diethyl (methoxy(4-nitrophenyl)methyl)phosphonate 
• 98450-81-8 (3E)-4-(4-nitrophenyl)-2-oxobut-3-enoic acid methyl ester 
• 1515-83-9 1-methoxymethyl-4-nitrobenzene 
• 555-16-8 4-nitrobenzaldehdye 

Relevant articles and documents

Synthesis of DPA-triazole structures and their application as ligand for metal catalyzed organic reactions

In this work, the use of DPA-triazole (DPA = dipicolylamine) molecules as ligands for metal catalyzed organic reactions has been investigated. A small library of ligands has been prepared by a CuAAC (click reaction) between propargyl-DPA and different azi

Preparation method of acetal or ketal compound

The invention discloses a preparation method of an acetal or ketal compound. The preparation method comprises the following steps: oscillating aldehyde or ketone, alcohol and a catalyst at 60 DEG C, and carrying out post-treatment after the reaction is finished to obtain the acetal compound, wherein the catalyst comprises alpha-chymotrypsin, the aldehyde or ketone has a structure represented by acompound A, R1 and R2 are respectively and independently selected from aryl, H and alkyl, the alcohol has a structure represented by a compound B, and R3 is selected from saturated alkane. The preparation method provided by the invention is catalyzed by alpha-chymotrypsin, is mild in reaction condition, simple in operation process, low in cost and environment-friendly, and has popularization and application values.

Synthesis, structural determination and catalytic study of a new 2-D chloro-substituted zinc phosphate, (C8N2H20)[ZnCl(PO3(OH))]2

A novel chloro-substituted zinc-phosphate, (C8N2H20)[ZnCl(PO3(OH))], has been synthesized by a slow evaporation method in the presence of 1,3-cyclohexanebis- (methylamine), which acts as a template. The structure consists of vertex linked ZnO3Cl and PO3(OH) tetrahedral, assembled into corrugated porous layers [ZnCl(PO3(OH))2]∞ with (4.82) topology. The optical properties were also investigated using Diffuse Reflecting Spectroscopy (DRS), showing that the title compound has semiconducting properties. In addition, the catalytic activity of (C8N2H20)[ZnCl(PO3(OH))]2 has been tested in the acetalisation reaction of aldehydes. The title compound displayed a high catalytic activity with practically total conversion in many examples using MeOD as solvent and as the sole source of acetalisation. More importantly, the reaction crudes are very clean and only the preferred products are found in the NMR spectra.