5736-90-3

Basic information

• Product Name: 1-(4-BUTOXYPHENYL)PROPAN-1-ONE
• Synonyms: 1-(4-BUTOXYPHENYL)PROPAN-1-ONE
• CAS NO: 5736-90-3
• Molecular Formula: C₁₃H₁₈O₂
• Molecular Weight: 206.28082
• Mol File: 5736-90-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(4-BUTOXYPHENYL)PROPAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-BUTOXYPHENYL)PROPAN-1-ONE(5736-90-3)
• EPA Substance Registry System: 1-(4-BUTOXYPHENYL)PROPAN-1-ONE(5736-90-3)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 5736-90-3(Hazardous Substances Data)

Usage

General Description

1-(4-BUTOXYPHENYL)PROPAN-1-ONE, also known as p-tert-butylpropiophenone, is a chemical compound with the molecular formula C13H18O2. It is a ketone compound that is commonly used in the synthesis of pharmaceuticals and organic compounds. It is a clear, colorless liquid that is soluble in organic solvents. This chemical is a key intermediate in the production of various chemicals and is used in the manufacturing of fragrances, flavors, and other organic compounds. It is important to handle this chemical with care, as it can be harmful if ingested, inhaled, or absorbed through the skin.

Upstream product

• 1126-79-0 n-butyl phenyl ether 
• 79-03-8 propionyl chloride 
• 542-69-8 1-iodo-butane 
• 70-70-2 4-hydroxypropiophenone 
• 36160-80-2 1-butoxy-4-(1-methylpropyl)benzene 
• 99-71-8 4-(1-methylpropyl)phenol 

Downstream Products

• 95558-94-4 1-(4-butoxy-phenyl)-2-methyl-3-piperidino-propan-1-one; hydrochloride 
• 354539-58-5 2-(4-butoxy-phenyl)-3-methyl-quinoline-4-carboxylic acid 
• 354539-57-4 6-bromo-2-(4-butoxy-phenyl)-3-methyl-quinoline-4-carboxylic acid 
• 102312-88-9 1-(4-butoxy-phenyl)-propan-1-one oxime 
• 92101-32-1 1-(4-Butyloxy-phenyl)-propanol-⁽¹⁾ 
• 115513-82-1 N-[1-(4-Butoxy-phenyl)-propyl]-N-hydroxy-acetamide 
• 98579-80-7 (2-Diethylamino-ethyl)-<1-(4-butyloxy-phenyl)-propyl>-ether 
• 92018-52-5 2-Bromo-1-(4-butoxy-phenyl)-propan-1-one 
• 586-60-7 dyclonine 

Relevant articles and documents

Site-Specific Oxidation of (sp3)C-C(sp3)/H Bonds by NaNO2/HCl

A site-specific oxidation of (sp3)C-C(sp3) and (sp3)C-H bonds in aryl alkanes by the use of NaNO2/HCl was explored. The method is chemical-oxidant-free, transition-metal-free, uses water as the solvent, and proceeds under mild conditions, making it valuable and attractive to synthetic organic chemistry.

Pyrazole and Isoxazole Derivatives as New, Potent, and Selective 20-Hydroxy-5,8,11,14-eicosatetraenoic Acid Synthase Inhibitors

In a previous paper, we reported the N-hydroxyformamidine derivative HET0016 as a potent and selective 20-HETE synthase inhibitor. Despite its attraction as a potential therapeutic agent for cerebral diseases, the preparation of an injectable formulation