CAS 62023-63-6

Fórmula: 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

Clave InChI: LDSJMFGYNFIFRK-DTWKUNHWSA-N

SMILES: C1=CC=C(C=C1)C[C@@H]([C@H](C(=O)O)O)N

(2R,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid

CAS: 62023-63-6

Pureza: 98%

Forma y color: Solid

Peso molecular: 195.2180023

Ref: 10-F611333

(2R,3S)-3-Amino-2-Hydroxy-4-Phenylbutanoic Acid

CAS: 62023-63-6

(2R,3S)-3-Amino-2-Hydroxy-4-Phenylbutanoic Acid

Fórmula: C₁₀H₁₃NO₃

Pureza: 99%

Forma y color: Solid

Peso molecular: 195.22

Ref: 54-OR1007985

(2R,3S)-3-Amino-2-Hydroxy-4-Phenylbutanoic Acid

CAS: 62023-63-6

Fórmula: C₁₀H₁₃NO₃

Pureza: 98%

Forma y color: Solid

Peso molecular: 195.2151

Ref: IN-DA00EILK

Bestatin Impurity 1

CAS: 62023-63-6

Fórmula: C₁₀H₁₃NO₃

Peso molecular: 195.22

Ref: 4Z-B-119004

(2R,3S)-3-Amino-2-hydroxy-4-phenylbutanoic acid

CAS: 62023-63-6

(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.

Fórmula: C₁₀H₁₃NO₃

Pureza: Min. 95%

Forma y color: Powder

Peso molecular: 195.21 g/mol

Ref: 3D-MCA02363