42486-87-3

Basic information

• Product Name: Benzoyl chloride, 4-chloro-3,5-dinitro-
• CAS NO: 42486-87-3
• Molecular Formula: C7H2Cl2N2O5
• Molecular Weight: 265.009
• Mol File: 42486-87-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 4-chloro-3,5-dinitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 4-chloro-3,5-dinitro-(42486-87-3)
• EPA Substance Registry System: Benzoyl chloride, 4-chloro-3,5-dinitro-(42486-87-3)

Safety Data

• Hazardous Substances Data: 42486-87-3(Hazardous Substances Data)

Upstream product

• 41252-93-1 4-chloro-3,5-diiodobenzoic acid 
• 74-11-3 para-chlorobenzoic acid 
• 118-97-8 4-chloro-3,5-dinitrobenzoic acid 

Downstream Products

• 52129-70-1 4'-chloro-3',5'-dinitroacetophenone 
• 58263-53-9 isobutyl 3,5-dinitro-4-chlorobenzoate 
• 1295573-32-8 C₂₈H₃₆N₈O₁₆ 
• 1295573-31-7 C₂₀H₃₁N₅O₁₀ 
• 53882-39-6 diethyl N,N'-(5-acetyl-2-chloro-m-phenylene)dioxamate 
• 53882-37-4 N,N'-(5-acetyl-2-chloro-m-phenylene)dioxamic acid 
• 53882-38-5 4-chloro-3,5-diaminoacetophenone 
• 861298-98-8 4-methoxy-3,5-dinitro-benzoic acid amide 
• 1019-52-9 4-hydroxy-3,5-dinitrobenzoic acid 
• 750538-65-9 2-amino-6-benzoyl-4-nitrobenzimidazole 
• 133100-06-8 2,4-diamino-6-benzylbenzimidazole dihydrochloride 

Relevant articles and documents

Aromatic triazole foldamers induced by C-H...X (X = F, Cl) intramolecular hydrogen bonding

Aryl-triazole oligomers based on isobutyl 4-fluorobenzoate and isobutyl 4-chlorobenzoate were designed and synthesized. Crystal structure and 1H-1H NOESY experiments demonstrate that the oligomers adopt stable helical conformation, which are induced by C5-H...X-C (X = F, Cl) intramolecular hydrogen bonding between triazole protons and halogen atoms. The stabilities of the folded conformations are confirmed by DFT calculations, which show that each C5-H...F-C planar interaction lowers the energy by ～3 kcal mol-1 on average, and by ～1 kcal mol-1 when C5-H...Cl-C bridges are formed. The hydrogen-bonding networks are disrupted in competitive hydrogen-bonding media such as DMSO, generating the unfolded oligomers.

Synthesis of Polyfunctionalized Biphenyls as Intermediates for a New Class of Liquid Crystals

A series of hexa- and octasubstituted biphenyls containing halogen, amino, nitro, and propylthio substituents were prepared by metal-mediated convergent synthesis from halobenzene precursors. The Pd-assisted C-C coupling methods were ineffective in the fo

Synthesis, selective aldose reductase inhibitory profile and antihyperglycaemic potential of certain parabanic acid derivatives

Synthesis and aldose reductase inhibitory profile of certain parabanic acid derivatives 1a-p is described. Also, the antihyperglycaemic potential of these compounds was studied. The most active inhibitors in this series were compounds 1 g, 1p, and 1o which showed inhibitory activity, 36.6, 90 and 91% respectively, at concentration 1 × 10-4. Their IC50 were 2 × 10-6, 7.5 × 10-8 and 5 × 10-8, respectively. Compound 1o exhibited pronounced antihyperglycaemic effect.