37062-67-2

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

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

Relevant academic research and scientific papers

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.

The coloring composition, a color filter, a manufacturing method of a color filter, an image display device, solid-state imaging device, and, a new compound and its tautomer

PROBLEM TO BE SOLVED: To provide a coloring composition having high solubility in organic solvents, high color purity, capable of providing high absorbance index with a thin layer, excellent in fastness (especially heat resistance and light resistance) an

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

A general and efficient catalyst for palladium-catalyzed C-O coupling reactions of aryl halides with primary alcohols

An efficient procedure for palladium-catalyzed coupling reactions of (hetero)aryl bromides and chlorides with primary aliphatic alcohols has been developed. Key to the success is the synthesis and exploitation of the novel bulky di-1-adamantyl-substituted bipyrazolylphosphine ligand L6. Reaction of aryl halides including activated, nonactivated, and (hetero)aryl bromides as well as aryl chlorides with primary alcohols gave the corresponding alkyl aryl ethers in high yield. Noteworthy, functionalizations of primary alcohols in the presence of secondary and tertiary alcohols proceed with excellent regioselectivity.

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.

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

Mesomorphic properties of 1-(4'-dodecylbiphenyl-4-yl)-3-(2 or 3-alkoxyphenyl)propane-1,3-diones: the influence of alkoxysubstituent position

Two homologous series of β-diketones, viz. 1-(4'-dodecylbiphenyl-4-yl)-3-(2-alkoxyphenyl)propane-1,3-diones and 1-(4'-dodecylbiphenyl-4-yl)-3-(3-alkoxyphenyl)propane-1,3-diones have been synthesised.The mesomorphic behaviour of all the compounds has been investigated using optical polarising microscopy and differential scanning colorimetry.The enthalpies associated with the transitions of all the liquid crystalline materials have also been determined.The mesophases exhibited by these compounds are explained on the basis of the structural features associated with such compounds.