3558-73-4

Basic information

• Product Name: Benzoyl chloride, 3,5-dimethyl-4-nitro-
• CAS NO: 3558-73-4
• Molecular Formula: C9H8ClNO3
• Molecular Weight: 213.62
• Mol File: 3558-73-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 3,5-dimethyl-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 3,5-dimethyl-4-nitro-(3558-73-4)
• EPA Substance Registry System: Benzoyl chloride, 3,5-dimethyl-4-nitro-(3558-73-4)

Safety Data

• Hazardous Substances Data: 3558-73-4(Hazardous Substances Data)

Upstream product

• 3095-38-3 3,5-dimethyl-4-nitrobenzoic acid 
• 603-71-4 nitromesitylene 

Downstream Products

• 19023-45-1 3,5-dimethyl-4-nitro-benzoic acid amide 
• 22978-16-1 N-Cyanomethyl-3,5-dimethyl-4-nitro-benzamide 
• 1044872-68-5 C₁₈H₁₇N₃O₅ 
• 1044871-31-9 2-(4-amino-3,5-dimethylphenyl)-5,7-dimethoxyquinazolin-4(3H)-one 
• 1044874-34-1 C₁₈H₁₉N₃O₆ 
• 108885-20-7 4-(N,N-diethyl-glycylamino)-3,5-dimethyl-benzoic acid amide 
• 109512-78-9 4-(2-chloro-acetylamino)-3,5-dimethyl-benzoic acid amide 
• 103796-44-7 4-amino-3,5-dimethyl-benzoic acid amide 
• 89210-38-8 4-benzyl-2,6-dimethylbenzenamine hydrochloride 
• 89210-37-7 3,5-dimethyl-4-nitrobenzhydrol 
• 112740-74-6 4-amino-N-[2-(dimethylamino)ethyl]-3,5-dimethylbenzamide 
• 80539-15-7 4-amino-3,5-dimethylacetophenone 2,6-dimethylphenylhydrazone 
• 80539-08-8 3,5-dimethyl-4-aminoacetophenone 
• 109306-95-8 4-Acetylamino-N-(2,6-dimethyl-phenyl)-3,5-dimethyl-benzamide 

Relevant articles and documents

Intramolecular electron transfer reactions in meso-(4-nitrophenyl)-substituted subporphyrins

A2B-type meso-(4-nitrophenyl)-substituted subporphyrins have been synthesized and shown to undergo very fast photoinduced intramolecular charge separation (CS) and charge recombination (CR) between the subporphyrin core and the meso-4-nitrophenyl group in CH2Cl2 as probed by femtosecond time-resolved transient absorption spectroscopy. Red-shifted emissions were detected from charge-separated states as a rare case for porphyrinoids.

COMPOUNDS FOR THE PREVENTION AND TREATMENT OF CARDIOVASCULAR DISEASES

The present disclosure relates to compounds, which are useful for regulating the expression of apolipoprotein A-I (ApoA-I), and their use for treatment and prevention of cardiovascular disease and related disease states, including cholesterol- or lipid-related disorders, such as, for example, atherosclerosis.

Synthesis and binding studies of bowl-shaped hosts for quaternary ammoniums

Two bowl-shaped hosts for quaternary ammonium salts were synthesized and their binding properties, along with the anion effect, were systematically examined and compared in CDCl3.