Ecenofloxacin

(+)-Limonene 1,2-epoxide, a monoterpene that can be prepared from (+)-limonene. It shows potent antinociceptive and antitumoral activity and is mainly used as a building block in synthesis of pharmaceutical products, perfumes, cosmetics and food

1,2-Epoxy-3-phenoxypropane

1,2-Epoxy-3-phenoxypropane

1,2-Epoxy-3-phenoxypropane

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

Application 2&#8242,7&#8242-Bis(2-carboxyethyl)-5(6)-carboxyfluorescein acetoxymethyl ester has been used for the estimation of vacuolar pH and intracellular pH. Biochem/physiol Actions An intracellular fluorescent pH indicator.

Application 3-Ethoxymethacrolein was used in the synthesis of: 5,10-dideaza-5,6,7,8-tetrahydrofolic acid (DDATHF) quinolines via modified Friedlander synthesis 3-[2-isopropyl-5-methylcyclohexyloxy-(1 R , 2 S , 5 R )]-2-methyl-2 E -propenal

6-Hydroxyflavanone is a flavonoid. Its biotransformation by Aspergillus niger strains have been described.

Application 7-Hydroxyflavanone has been used for the stereoisomeric separation of flavonoids using polysaccharide-based chiral stationary phases by nano-liquid chromatography (nano-LC).

Application Reactant: Acting as a biologically valuable acceptor in O -glycosidation reactions Involved in synthesis of fully phosphorylated flavones for use as pancreatic cholesterol esterase inhibitors For O -methylation with di-Me carbonate