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Home/Compounds/Research Reagent/(2S)-2-amino-3-phenyl-1-propanol
C9H13NO
151.21 g/mol
Research ReagentDanger

PHENYLALANINOL, (R)-

CAS5267-64-1EC226-086-1
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound

(R)-Phenylalaninol is a chiral amino alcohol derivative of phenylalanine. It is primarily used as a research compound and a building block in peptide synthesis.

research compoundbuilding block in peptide synthesis

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

ReferenceSame Category

4-Amino-3-chlorophenol hydrochloride

CAS52671-64-4

research compound

ReferenceSame Category

1,1,1-Trimethoxy-2-methylpropane

CAS52698-46-1

research compound

ReferenceSame Category

Azomycin

CAS527-73-1

research compound

ReferenceSame Category

2-Bromo-3-pyridinecarboxylic acid methyl ester

CAS52718-95-3

research compound

Referencestereoisomer of

L-phenylalaninol

CAS3182-95-4

research compound

Safety Reference

Corrosive
Corrosive
Danger
H314Causes severe skin burns and eye damage

Customs Tariff Classification

The international HS code for PHENYLALANINOL, (R)- (CAS 5267-64-1) is 2922.19.

HS code (international, 6-digit)

2922.19

EU CN code (8-digit)

2922 19 00

Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.

Identifiers
IUPAC Name

(2R)-2-amino-3-phenylpropan-1-ol

InChIKey

STVVMTBJNDTZBF-SECBINFHSA-N

SMILES

C1=CC=C(C=C1)C[C@H](CO)N

Synonyms (20)
  • (R)-2-Amino-3-phenylpropanol
  • (R)-BENZYLGLYCINOL
  • (R)-PHENYLALANINOL
  • 2-Amino-3-phenyl-1-propanol #
  • D-Penylalaninol
  • D-Phenylalaninol
  • PHENYLALANINOL, (R)-
  • Phenylalaninol, D-
  • SOLRIAMFETOL METABOLITE M8

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