
CAS 62023-63-6
:Formule :C10H13NO3
InChI :InChI=1S/C10H13NO3/c11-8(9(12)10(13)14)6-7-4-2-1-3-5-7/h1-5,8-9,12H,6,11H2,(H,13,14)/t8-,9+/m0/s1
Code InChI :LDSJMFGYNFIFRK-DTWKUNHWSA-N
SMILES :C1=CC=C(C=C1)C[C@@H]([C@H](C(=O)O)O)N
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(2R,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid
CAS :Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :195.2180023(2R,3S)-3-Amino-2-Hydroxy-4-Phenylbutanoic Acid
CAS :(2R,3S)-3-Amino-2-Hydroxy-4-Phenylbutanoic AcidFormule :C10H13NO3Degré de pureté :99%Couleur et forme :SolidMasse moléculaire :195.22(2R,3S)-3-Amino-2-Hydroxy-4-Phenylbutanoic Acid
CAS :Formule :C10H13NO3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :195.2151(2R,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid
CAS :(2R,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid is an enantiomerically pure amino acid that is used in the synthesis of chiral drugs. It is a solid that can be synthesized by reacting (2S)-3-amino-2-hydroxypropanoic acid with phenyl boronic acid and potassium carbonate in a high diastereoselectivity reaction. This compound has been shown to have high diastereoselectivity in its alkylation reactions, which makes it useful for the synthesis of chiral drugs.Formule :C10H13NO3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :195.21 g/mol





