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BOC-DL-PHE-OH

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Products Intro: Product Name:Boc-DL-Phe-OH
CAS:4530-18-1
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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CAS:4530-18-1
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CAS:4530-18-1
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Products Intro: Product Name:Boc-DL-Phenylalanine
CAS:4530-18-1
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Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:n-methyl-boc-d-phenylalanine
CAS:4530-18-1
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BOC-DL-PHE-OH manufacturers

  • BOC-DL-PHE-OH
  • BOC-DL-PHE-OH pictures
  • $3.00 / 1KG
  • 2020-01-13
  • CAS:4530-18-1
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 200KG
BOC-DL-PHE-OH Basic information
Product Name:BOC-DL-PHE-OH
Synonyms:BOC-DL-PHENYLALANINE;BOC-DL-PHE-OH;N-ALPHA-T-BUTOXYCARBONYL-D-PHENYLALANINE;N-tert-Butoxycarbonyl-DL-phenylalanine;N-Methyl-Boc-D-phenylalanine;Boc-N-Me-Phe-OH;BOC-DL-Phenylalanine(Boc-DL-Phe-OH);2-(tert-butoxycarbonyl(Methyl)aMino)-3-phenylpropanoic acid
CAS:4530-18-1
MF:C14H19NO4
MW:265.3
EINECS:1533716-785-6
Product Categories:Phenylalanine [Phe, F]
Mol File:4530-18-1.mol
BOC-DL-PHE-OH Structure
BOC-DL-PHE-OH Chemical Properties
Melting point 106-108 °C
Boiling point 426.6±38.0 °C(Predicted)
density 1.160±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
pka3.88±0.10(Predicted)
form Solid
color White to off-white
CAS DataBase Reference4530-18-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 43
Safety Statements 36/37
HS Code 29224999
MSDS Information
BOC-DL-PHE-OH Usage And Synthesis
Uses2-(tert-butoxycarbonylamino)-3-phenylpropanoic acid is a phenylalanine derivative[1].
Synthesis
DL-Phenylalanine

150-30-1

Di-tert-butyl dicarbonate

24424-99-5

BOC-DL-PHE-OH

4530-18-1

General procedure for the synthesis of 2-((tert-butoxycarbonyl)amino)-3-phenylpropionic acid from DL-phenylalanine and di-tert-butyl dicarbonate: DL-phenylalanine (1 g, 6.05 mmol) was suspended in a mixture of dioxane (15 mL) and NaOH (2M aqueous solution; 3.63 mL, 7.26 mmol) at 0 °C. Subsequently, di-tert-butyl dicarbonate (1.546 mL, 6.66 mmol) was added slowly and dropwise to this suspension. The reaction mixture was stirred continuously for 5 hours at room temperature. Upon completion of the reaction, the mixture was concentrated under vacuum to remove the solvent. Water (30 mL) was added to the concentrate and the pH of the mixture was adjusted to 3 by dropwise addition of cold 1.5 N HCl solution.The aqueous layer was extracted with ethyl acetate (3 x 50 mL) and the organic layers were combined and washed with brine solution (2 x 50 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated to afford the target product 2-((tert-butoxycarbonyl)amino)-3-phenylpropanoic acid (1.3 g, 4.90 mmol, 81% yield) as a gelatinous liquid. The product was confirmed by 1H NMR (400 MHz, DMSO-d6) and mass spectrometry (ESI): 1H NMR δ 12.6 (br-s, 1H), 7.32-7.26 (m, 5H), 7.10-6.95 (br-s, 1H), 4.12-4.00 (m, 1H), 3.05-2.92 (m, 1H), 2.87- 2.75 (m, 1H), 1.31 (s, 9H); MS (ESI) m/z 266.2 [M+H]+.

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):1793-882. DOI:10.1080/10408398.2012.708368
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