Molecular Biology Reagents

5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol.

5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol.

5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol.

5-Chloro-2-hydroxyisophthalaldehyde.

5-Chloro-2-methylphenol (5-chloro- o -cresol) can be synthesized from 5-chloro-2-methylaniline. 5-Chloro-2-methylphenol is formed as one of the hydroxylation reaction products of p -chlorotoluene.

5-Ethyl-2-methoxyphenol.

Application 5-Hexenoic acid may be used for the preparation of iodolactone derivatives and fluorine-containing &#948-valerolactones.

Application 5-Hexenoic acid may be used for the preparation of iodolactone derivatives and fluorine-containing &#948-valerolactones.

Analysis Note Assay (GC, area%): &#8805 97.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

Analysis Note Assay (GC, area%): &#8805 97.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

A cell permeable, bioavailable, 2-indolealkanoic acid derived compound that acts as a highly potent and selective inhibitor of leukotriene biosynthesis (IC 50 = 3.1 nM in intact human polymorphonuclear leukocytes).

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.