Methylphenidate

rest mainly 3-methyl-1-butanol Application ( S )-(-)-2-Methylbutanol can be used as a reactant to prepare: Methylbutyl-2-(3-thienyl)acetate (MBTA) by esterification reaction with 3-thiophene acetic acid in the presence of an acid catalyst. (2 S

Application ( S )-(&#8722)-2-Methylbutanol can be used to prepare: ( S )-(&#8722)-2-Methyl-1-butyloxy carbonyl amino hexyl isocyanate (MBI), which is used to synthesize isocyanate copolymers. Chiral alkoxynaphathoic acid derivatives having liquid

Application ( S )-(-)-&#945-Methylbenzylamine along with 2-formylphenylboronic acid has been used in a derivatization protocol to analyze the enantiomeric excess of chiral diols. It can also be used: In the diastereoselective synthesis of S

Application ( S )-(-)-&#945-Methylbenzylamine along with 2-formylphenylboronic acid has been used in a derivatization protocol to analyze the enantiomeric excess of chiral diols. It can also be used: In the diastereoselective synthesis of S

(S)-3-Methylbutan-2-Ol .

(S)-3-Methylbutan-2-Ol .

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.

(S)-6-Methylhept-5-en-2-ol.

(S)-6-Methylhept-5-en-2-ol.

(S)-6-Methylhept-5-en-2-ol.

(S)-8a-Methyl-3,4,8,8a-tetrahydronaphthalene-1,6(2H,7H)-dione.

(S)-8a-Methyl-3,4,8,8a-tetrahydronaphthalene-1,6(2H,7H)-dione.