37062-67-2

Basic information

• Product Name: Ethanone, 1-(3-butoxyphenyl)-
• CAS NO: 37062-67-2
• Molecular Formula: C12H16O2
• Molecular Weight: 192.258
• Mol File: 37062-67-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(3-butoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3-butoxyphenyl)-(37062-67-2)
• EPA Substance Registry System: Ethanone, 1-(3-butoxyphenyl)-(37062-67-2)

Safety Data

• Hazardous Substances Data: 37062-67-2(Hazardous Substances Data)

Upstream product

• 542-69-8 1-iodo-butane 
• 121-71-1 3-Hydroxyacetophenone 
• 109-69-3 n-Butyl chloride 
• 2142-63-4 1-(3-Bromophenyl)ethanone 
• 71-36-3 butan-1-ol 
• 109-65-9 1-bromo-butane 

Downstream Products

• 1156342-21-0 C₁₂H₁₈O₂ 
• 115513-94-5 N-[1-(3-Butoxy-phenyl)-ethyl]-N-hydroxy-acetamide 
• 1020974-56-4 1-(3-Butoxy-phenyl)-ethanone oxime 

Relevant articles and documents

2-AMINO-1,3,4-THIADIAZINE AND 2-AMINO-1,3,4-OXADIAZINE BASED ANTIFUNGAL AGENTS

The invention provides a compound which is a diazine of formula (I) or a tautomer thereof, or a pharmaceutically acceptable salt thereof, for use as an antifungal agent: (I) wherein X, N', C', A and E are as defined herein. The invention also provides a compound of Formula (I) as defined herein.

Synthesis, characterization and photochromism of 3′-butoxyflavylium derivatives

The compounds 3′-butoxy-7-methoxyflavylium and 3′-butoxy-7- hydroxyflavylium were synthesized and the respective equilibrium and rate constants determined by two complementary techniques, pH jumps and flash photolysis. An experimental strategy based on th

Reactivity in micelles - Are we really able to design micellar catalysts?

Coordination of lipophilic alkyl pyridin-2-yl ketoximes 1 to Ni 2+ ions, reduction of lipophilic 3-alkoxyacetophenones 2 with sodium borohydride, and alkaline hydrolysis of 4-nitrophenyl diphenyl phosphate (PNPDPP) were employed as probes in the investigation which factors may influence the reactivity of organic compounds in micellar systems. In all these reactions, a lipophilic substrate solubilized in micellar core was attacked by a hydrophilic reagent from the bulk aqueous phase. To evaluate the contribution of electrostatic interactions between the micellar surface charge and the reagent to the observed reactivity, we combined reactions involving the reagents with opposite polarity (Ni2+ cations and borohydride or hydroxide anions) with positively charged micelles of hexadecyltrimethyl-ammonium chloride (CTAC) or bromide (CTAB) and negatively charged micelles of sodium dodecyl sulfate (SDS). Non-ionic micelles (Triton X-100 or Brij 35) served as a reference. The results of the kinetic studies give evidence that each of the investigated systems has unique properties going in particular aspects beyond the scope of the generally accepted concepts of reactivity in micelles.