CAS 33125-05-2
:boc-D-alpha-phenylglycin
- Boc-D-Phg-OH
- N-(tert-Butoxycarbonyl)-D-phenylglycine
- Boc-D-phenylglycine
- N-(tert-butoxycarbonyl)-N-phenylglycine
N-(tert-Butoxycarbonyl)-D-2-phenylglycine
CAS:Formel:C13H17NO4Reinheit:>98.0%(T)(HPLC)Farbe und Form:White to Almost white powder to crystalMolekulargewicht:251.28N-Boc-D-phenylglycine, 99%
CAS: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)phenylacetic acid. R)--[[(1,1-Dimethylethoxy)carbonyl]amino]-benzeneacetic Acid is D-(+)-2-Phenylglycine with Boc protec
Formel:C13H17NO4Reinheit:99%Farbe und Form:White, PowderMolekulargewicht:251.28Ref: IN-DA00393S
1gNachfragen5g24,00€10g24,00€1kg186,00€25g30,00€5kgNachfragen100g54,00€10kgNachfragen500g128,00€N-Boc-D-phenylglycine
CAS:N-Boc-D-phenylglycine is an organic compound that is used in the asymmetric synthesis of pyrazoles. It has been shown to react with ketones to form β-unsaturated ketones in a reaction mechanism that involves the formation of an imine intermediate. N-Boc-D-phenylglycine can be synthesized by reacting phenylacetic acid with D,L-alanyl chloride followed by hydrolysis and reaction with ammonia. The compound can also be made from pyrazole and Boc anhydride. N-Boc-D-phenylglycine is soluble in organic solvents such as chloroform and THF but not water, making it useful for organic synthesis under solvent conditions. It is orally bioavailable and can be administered to humans without any toxic effects.
Formel:C13H17NO4Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:251.28 g/molBoc-D-Phg-OH
CAS:M03222 - Boc-D-Phg-OH
Formel:C13H17NO4Reinheit:98%Farbe und Form:SolidMolekulargewicht:251.282(AlphaR)-Alpha-[[(1,1-Dimethylethoxy)carbonyl]amino]-benzeneacetic Acid
CAS:Kontrolliertes ProduktFormel:C13H17NO4Farbe und Form:NeatMolekulargewicht:251.28








