CAS 132201-32-2: Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride (1:1), (αR,βS)-
Formula:C9H11NO3·ClH
InChI:InChI=1S/C9H11NO3.ClH/c10-7(8(11)9(12)13)6-4-2-1-3-5-6;/h1-5,7-8,11H,10H2,(H,12,13);1H/t7-,8+;/m0./s1
InChI key:InChIKey=OTJZSGZNPDLQAJ-KZYPOYLOSA-N
SMILES:[C@H]([C@H](C(O)=O)O)(N)C1=CC=CC=C1.Cl
Synonyms:- (1S,2R)-2-carboxy-2-hydroxy-1-phenylethanaminium chloride
- (2R,3S)-3-Amino-2-Hydroxy-3-Phenyl-Propanoic Acid Hydrochloride
- (2R,3S)-3-Amino-2-hydroxy-3-phenyl-propanoic acid
- (2R,3S)-3-Amino-2-hydroxy-3-phenylpropanic acid
- (2R,3S)-3-Phenylisoserine hydrochloride
- (2R,3S)-3-ammonio-2-hydroxy-3-phenylpropanoate
- (2R,3S)-Phenylisoserine Hydrochloride
- 3-(2R,3S)-Phenylisoserine
- Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride (1:1), (αR,βS)-
- Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride, (αR,βS)-
- Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride, [R-(R*,S*)]-
- See more synonyms
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Found 12 products.
(2R,3S)-3-Amino-2-hydroxy-3-phenylpropanoic Acid Hydrochloride
CAS:Controlled ProductFormula:C9H11NO3·ClHColor and Shape:NeatMolecular weight:217.65(2R,3S)-3-Phenylisoserine hydrochloride
CAS:"(2R,3S)-3-Phenylisoserine hydrochloride serves as a pharmaceutical intermediate."Formula:C9H12ClNO3Purity:≥95%Color and Shape:SolidMolecular weight:217.65(2R,3S)-3-Phenylisoserine hydrochloride
CAS:(2R,3S)-3-Phenylisoserine hydrochloridePurity:≥98%Molecular weight:217.65g/molDocetaxel Related Compound 1 HCl ((2R, 3S)-3-Phenylisoserine HCl)
CAS:Formula:C9H11NO3·HClColor and Shape:White To Off-White SolidMolecular weight:181.19 36.46Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride (1:1), (αR,βS)-
CAS:Formula:C9H12ClNO3Purity:97%Color and Shape:SolidMolecular weight:217.64948(2R,3S)-3-Amino-2-hydroxy-3-phenylpropanoic acid hydrochloride
CAS:(2R,3S)-3-Amino-2-hydroxy-3-phenylpropanoic acid hydrochloride is an organic compound that is used in the manufacture of taxol, an anticancer drug. It is synthesized by reacting chloroacetic acid with a metal hydroxide, such as sodium hydroxide or potassium hydroxide. The reaction proceeds spontaneously to form the enantiomerically pure (2R,3S) form and unreacted (2S,3R) form. The (2R,3S) enantiomer has been found to be more reactive than the (2S,3R) form. Quaternary ammonium salts are formed when the (2R,3S) enantiomer reacts with quaternary ammonium compounds such as benzyltrimethylammonium chloride. This compound can also be used in catalytic reactions to produce drugs such as carbapenems and penFormula:C9H12ClNO3Purity:Min. 95%Molecular weight:217.65 g/mol(2R,3S)-3-Phenylisoserine hydrochloride
CAS:(2R,3S)-3-Phenylisoserine hydrochlorideFormula:C9H11NO3·ClHPurity:98+%Color and Shape: white powderMolecular weight:217.65g/mol
