N-Boc-D-苯基甘氨酸

It is a reagent of choice for assignment of absolute configuration of chiral primary amines by 1H NMR, giving better results than Mosher's acid ((R)-(+)-?-Methoxy-?-(trifluoromethyl)?-phenyl?-acetic acid. αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]-benzeneacetic Acid is D-(+)-2-Phenylglycine with Boc protecting group. (αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]-benzeneacetic Acid is used as part of a catalyst combination to catalyze regioselective [4 + 2] cycloadditions of β-substituted cyclic enones and polyconjugated malononitriles. It can also be used to catalyze stereoselective preparation of polyfunctional nitrocyclohexene carboxaldehydes.

Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.

MFCD00062043

C₁₃H₁₇NO₄

251.28

90-92°

Keep Cold.

Powder

Insoluble in water. Slightly soluble in DMSO and methanol.

3033982

否