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H-4-NITRO-PHE-OET HCL

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H-4-NITRO-PHE-OET HCL manufacturers

  • 4-NO2-Phe-Oet.HCl
  • 4-NO2-Phe-Oet.HCl pictures
  • 2026-09-11
  • CAS:58816-66-3
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
H-4-NITRO-PHE-OET HCL Basic information
Product Name:H-4-NITRO-PHE-OET HCL
Synonyms:P-NITRO-L-PHENYLALANINE ETHYL ESTER HYDROCHLORIDE;ETHYL (S)-2-AMINO-3-(4-NITROPHENYL)PROPANOIATE;H-PHE(4-NO2)-OET HCL;H-4-NITRO-PHE-OET HCL;4-NITRO-L-PHENYLALANINE ETHYL ESTER HYDROCHLORIDE;ethyl 4-nitro-3-phenyl-L-alaninate monohydrochloride;3-(4-NITRO-PHENYL)-L-ALANINE ETHYL ESTER HCL;p-Nitrophenylalanine ethyl ester hydrochloride
CAS:58816-66-3
MF:C11H15ClN2O4
MW:274.7
EINECS:261-455-0
Product Categories:Phenylalanine [Phe, F]
Mol File:58816-66-3.mol
H-4-NITRO-PHE-OET HCL Structure
H-4-NITRO-PHE-OET HCL Chemical Properties
Melting point 177-180 °C
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO:PBS (pH 7.2) (1:3): 0.25mg/mL
form A crystalline solid
color White to off-white
Safety Information
MSDS Information
H-4-NITRO-PHE-OET HCL Usage And Synthesis
Uses3-(4-Nitro-phenyl)-L-alanine ethyl ester hydrochloride is an alanine derivative[1].
Synthesis
4-Nitro-3-phenyl-L-alanine

949-99-5

H-4-NITRO-PHE-OET HCL

58816-66-3

Thionyl chloride (21 mL, 0.29 mol) was slowly added dropwise to 500 mL of anhydrous ethanol at 0 °C and under nitrogen protection for a controlled time of 5 min. After the dropwise addition, the clarified reaction solution was continued to be stirred at 0 °C for 10 min, and then brought to room temperature and stirred for 30 min. A one-time addition of 4-nitro-L-phenylalanine (50.2 g, 0.24 mol) was added to the reaction system and the mixture was heated to reflux overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure to afford ethyl (S)-2-amino-3-(4-nitrophenyl)propionate hydrochloride (60 g, 92% yield) as a white solid. The product was characterized by 1H NMR (400 MHz, CD3OD): δ 8.21 (d, 2H), 7.54 (d, 2H), 4.39 (dd, 1H), 4.22 (q, 2H), 3.24-3.40 (m, 2H), 1.22 (t, 3H).

References[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368
H-4-NITRO-PHE-OET HCL Preparation Products And Raw materials
Raw materials4-Nitro-3-phenyl-L-alanine
Tag:H-4-NITRO-PHE-OET HCL(58816-66-3) Related Product Information
4-Amino-L-phenylalanine hydrochloride L-4-Nitrophenylalanine methyl ester hydrochloride L-4-Benzoylphenylalanine Phe-Gly-Gly H-Phe(4-Cl)-OMe.HCl METHYL 4-BROMO-L-PHENYLALANINATE HYDROCHLORIDE L-4-Cyanophenylalanine 4-AMINOTETRAHYDROPYRAN-4-CARBOXYLIC ACID METHYL ESTER HYDROCHLORIDE H-Phe-D-Phe-OMe.HCl L-4-TERT-BUTYL-PHE L-4-Fluorophenylalanine L-4-Chlorophenylalanine 4-Methoxy-L-phenylalanine L-4-Iodophenylalanine 4-Methylphenyl-L-alanine H-Phe-Ala-OH ETHYL 4-NITRO-L-PHENYLALANINE 4-NITRO-PHENYLALANINE METHYL ESTER