CAS 33125-05-2
:boc-D-alfa-fenilglicina
- Boc-D-Phg-OH
- N-(tert-Butoxycarbonyl)-D-phenylglycine
- Boc-D-phenylglycine
- N-(tert-butoxycarbonyl)-N-phenylglycine
N-(tert-Butoxycarbonyl)-D-2-phenylglycine
CAS:Fórmula:C13H17NO4Pureza:>98.0%(T)(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular: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
Fórmula:C13H17NO4Pureza:99%Forma y color:White, PowderPeso molecular:251.28Ref: IN-DA00393S
1gA consultar5g24,00€10g24,00€1kg186,00€25g30,00€5kgA consultar100g54,00€10kgA consultar500g128,00€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.
Fórmula:C13H17NO4Pureza:Min. 95%Forma y color:PowderPeso molecular:251.28 g/molBoc-D-Phg-OH
CAS:M03222 - Boc-D-Phg-OH
Fórmula:C13H17NO4Pureza:98%Forma y color:SolidPeso molecular:251.282(AlphaR)-Alpha-[[(1,1-Dimethylethoxy)carbonyl]amino]-benzeneacetic Acid
CAS:Producto controladoFórmula:C13H17NO4Forma y color:NeatPeso molecular:251.28








