H-Phe-NH2 · HCl

Name: H-Phe-NH2 · HCl | 65864-22-4
Brand: US-CATO
SKU: S57CPTD787955_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD787955_10_MG

Vendor: US-CATO

Product Information

Product Name

H-Phe-NH2 · HCl

Brand Name

US-CATO

Product Number

CPTD787955

CAS

65864-22-4

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

11953719

IUPAC Name

(2S)-2-amino-3-phenylpropanamide;hydrochloride

InChI Key

KLHLGTPNBQXSJT-QRPNPIFTSA-N

SMILES

C1=CC=C(C=C1)CC@@H(C(=O)N)N.Cl

References Data Source From Pubchem

Analysis and Enantioseparation of Amino Acids by Liquid Chromatography

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2019

DOI: 10.1007/978-1-4939-9639-1_17

Evaluation of carboxamide-type synthetic cannabinoids as CB1/CB2 receptor agonists: difference between the enantiomers

Publication Name: Forensic Toxicology

Publication Date: 2017-08-04

DOI: 10.1007/s11419-017-0378-5

Reversed-phase liquid chromatographic resolution of diastereomers of protein and non-protein amino acids prepared with newly synthesized chiral derivatizing reagents based on cyanuric chloride

Publication Name: Amino Acids

Publication Date: 2010-06-18

DOI: 10.1007/s00726-010-0650-z

Chromatographic separation of enantiomers of non-protein α-amino acids after derivatization with Marfey’s reagent and its four variants

Publication Name: Amino Acids

Publication Date: 2008-07-09

DOI: 10.1007/s00726-008-0135-5

Synthesis of polypeptides by microwave heating I. Formation of polypeptides during repeated hydration-dehydration cycles and their characterization

Publication Name: Journal of Molecular Evolution

Publication Date: 1990-09

DOI: 10.1007/bf02109494

H-Phe-NH2 · HCl

Product Information

General Information

References Data Source From Pubchem

Analysis and Enantioseparation of Amino Acids by Liquid Chromatography

Evaluation of carboxamide-type synthetic cannabinoids as CB1/CB2 receptor agonists: difference between the enantiomers

Reversed-phase liquid chromatographic resolution of diastereomers of protein and non-protein amino acids prepared with newly synthesized chiral derivatizing reagents based on cyanuric chloride

Chromatographic separation of enantiomers of non-protein α-amino acids after derivatization with Marfey’s reagent and its four variants

Synthesis of polypeptides by microwave heating I. Formation of polypeptides during repeated hydration-dehydration cycles and their characterization

H-Phe-NH2 · HCl

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H-Phe-NH2 · HCl

Product Information

General Information

References Data Source From Pubchem

Analysis and Enantioseparation of Amino Acids by Liquid Chromatography

Evaluation of carboxamide-type synthetic cannabinoids as CB1/CB2 receptor agonists: difference between the enantiomers

Reversed-phase liquid chromatographic resolution of diastereomers of protein and non-protein amino acids prepared with newly synthesized chiral derivatizing reagents based on cyanuric chloride

Chromatographic separation of enantiomers of non-protein α-amino acids after derivatization with Marfey’s reagent and its four variants

Synthesis of polypeptides by microwave heating I. Formation of polypeptides during repeated hydration-dehydration cycles and their characterization

H-Phe-NH2 · HCl

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