Application

N⁶-Methyladenosine 5'-monophosphate sodium salt can be used in N⁶-methyladenosine (m⁶A) ribonucleoprotein immunoprecipitation reactions. m6A has gained a lot of attention in the recent years because the mRNA modification with m6A has been shown to play a role in stability and translational efficiency of mRNA.

Used to prepare reagents for chiral vinylogous Darzens and Reformatsky reactions. Important chiral auxiliary employed in the resolution of acids and for stereocontrolled synthesis.

(1R,2S,5R)-(-)-Menthol may be used to synthesize: • chiral enantiopure 2-(1-hydroxyalkyl)pyridines, which can react with to form C3-symmetric tripodal ligands • menthylphosphorodichioridite, a chiral derivatizing agent for the determination of enantiomeric purity of chiral diols or diamines by ³¹P NMR spectroscopy • (2R,4S)-2,3,4,5-tetrahydro-2-(-)-menthyloxy-2-methyl-4-phenylpyrano-[3,2-c]-benzopyran-5-one, an intermediate to prepare a warfarin analog It may also be used as a chiral auxiliary, to induce chirality while synthesizing (-)-horsfiline.

Biochem/physiol Actions

A glycogen phosphorylase b activator.

General description

(1R,2S,5R)-(-)-Menthol is a monoterpene.

Legal Information

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Packaging

10 mg in glass bottle

25, 100, 500 g in poly bottle