7007-92-3

Basic information

• Product Name: Cetohexazine
• Synonyms: Cetohexazine;4,6-Dimethylpyridazin-3(2H)-one;4,6-Dimethylpyridazine-3-ol;Ketohexazine;4,6-dimethyl-2,3-dihydropyridazin-3-one;4,6-Dimethylpyridazin-3(2H)
• CAS NO: 7007-92-3
• Molecular Formula: C₆H₈N₂O
• Molecular Weight: 124.14
• Mol File: 7007-92-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Density: 1.17g/cm³
• Refractive Index: 1.563
• CAS DataBase Reference: Cetohexazine(CAS DataBase Reference)
• NIST Chemistry Reference: Cetohexazine(7007-92-3)
• EPA Substance Registry System: Cetohexazine(7007-92-3)

Safety Data

• Hazardous Substances Data: 7007-92-3(Hazardous Substances Data)

Usage

General Description

Cetohexazine is a chemical compound that is used as an antihistamine and sedative. It is commonly prescribed to treat allergies, hay fever, and other allergic reactions, as well as to relieve symptoms of anxiety and tension. Cetohexazine works by blocking the effects of histamine, a substance in the body that causes allergic symptoms, and by decreasing the activity of the central nervous system, leading to a calming and sedating effect. It is available in the form of oral tablets and should be taken as directed by a healthcare professional to ensure safe and effective use. Common side effects may include drowsiness, dizziness, and dry mouth, and it is important to avoid alcohol and certain medications while taking cetohexazine.

InChI:InChI=1/C6H8N2O/c1-4-3-5(2)7-8-6(4)9/h3H,1-2H3,(H,8,9)

Upstream product

• 50-00-0 formaldehyd 
• 1027102-66-4 4-diethoxyphosphoryl-6-methylpyridazin-3(2H)-one 
• 6641-83-4 2-methyl-4-oxopentanoic acid 
• 23227-96-5 4,5-dihydro-4,6-dimethylpyridazin-3(2H)-one 
• 81416-97-9 2-Hydroxy-4-oxo-2-methyl-pentansaeure 
• 35504-82-6 2-methyl-4-oxo-pent-2c-enoic acid 

Downstream Products

• 118269-99-1 (4,6-Dimethyl-pyridazin-3-yl)-(2-morpholin-4-yl-ethyl)-amine; hydrochloride 
• 17258-26-3 3-chloro-4,6-dimethylpyridazine 

Relevant articles and documents

New, simple and versatile synthesis of 4,6-disubstituted pyridazin-3(2H)-ones

A simple, two-step synthesis of 4,6-disubstituted pyridazin-3(2H)-ones starting from 2-diethoxyphosphoryl-4-oxoalkanoates and hydrazines is described. The intermediate 4-diethoxyphosphoryl-4,5-dihydropyridazin-3(2H)-ones obtained in this way are used in a

3-Aminopyridazine derivatives with atypical antidepressant, serotonergic, and dopaminergic activities

Minaprine [3[(β-morpholinoethyl)amino]4-methyl-6-phenylpyridazine dihydrochloride] is active in most animal models of depression and exhibits in vivo a dual dopaminomimetic and serotoninomimetic activity profile. In an attempt to dissociate these two effe