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 
• 24588-74-7 4-nitrophenyl-1,3-dithiane 
• 2403-62-5 p-nitrobenzaldehyde diethyl acetal 
• 1129-37-9 4-nitrobenzaldehyde oxime 
• 110-89-4 piperidine 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-13-0 4-nitrostyrene 
• 3048-12-2 4-nitrobenzyl phenyl ether 
• 456-27-9 4-nitrobenzenediazonium tetrafluoroborate 
• 536-74-3 phenylacetylene 

Downstream Products

• 3516-76-5 4-phenylazobenzaldehyde 
• 56377-72-1 (α-Chlor-4-nitrobenzyl)methylether 
• 93136-94-8 Methoxy-tert.-butylperoxy-<4-nitro-phenyl>-methan 
• 92594-60-0 diethyl (methoxy(4-nitrophenyl)methyl)phosphonate 
• 4578-70-5 p-nitrobenzaldehyde ethyl-methyl acetal 
• 151562-82-2 1,8-Dihydroxy-10-[methoxy (4-nitrophenyl)methyl]-9(10H)-anthracenone 
• 43186-44-3 2-(4-nitrophenyl)-4H-benzo[d][1,3]dioxin 
• 1086408-55-0 4,4'-((4-nitrophenyl)methylene)bis(1H-pyrrole-2-carbaldehyde) 
• 3156-41-0 1-nitro-4-[(E)-2-nitroeth-1-enyl]benzene 
• 555-16-8 4-nitrobenzaldehdye 
• 3156-41-0 1-nitro-4-(2-nitrovinyl)benzene 

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

Photochemical synthesis of acetals utilizing Schreiner's thiourea as the catalyst

Acetalization of aldehydes is an area of great importance in Organic Chemistry for both synthetic and biological puproses. Herein, we report a mild, inexpensive and green photochemical protocol, where Schreiner's thiourea (N,N′-bis[3,5-bis(trifluoromethyl)-phenyl]-thiourea) is utilized as the catalyst and cheap household lamps as the light source. A variety of aromatic and aliphatic aldehydes were converted into acetals in good to high yields (23 examples, 36-96% yield) and an example of the synthesis of a cyclic acetal is provided. The reaction mechanism was also studied.

α-Chymotrypsin-Induced Acetalization of Aldehydes and Ketones with Alcohols

This is the first report of a simple and general method for acetalization of aldehydes via an α-chymotrypsin-induced reaction under mild conditions. A broad range of aromatic and heteroaromatic aldehydes have been acetalized under neutral conditions in good yields using a catalytic amount of chymotrypsin.