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TERT-BUTOXYCARBONYLAMINO-PHENYL-ACETIC ACID

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TERT-BUTOXYCARBONYLAMINO-PHENYL-ACETIC ACID Basic information

Product Name:
TERT-BUTOXYCARBONYLAMINO-PHENYL-ACETIC ACID
Synonyms:
  • BOC-DL-PHG-OH
  • BOC-DL-(PHENYL)GLY-OH
  • tert-Butoxycarbonylphenylglycine
  • N-BOC-phenylglycine
  • BOC-Phg
  • Boc-DL-phenylglycine
  • TERT-BUTOXYCARBONYLAMINO-PHENYL-ACETIC ACID
  • RARECHEM AK ML 0503
CAS:
3601-66-9
MF:
C13H17NO4
MW:
251.28
EINECS:
1533716-785-6
Product Categories:
  • Amino Acids and Derivatives
  • Miscellaneous
Mol File:
3601-66-9.mol
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TERT-BUTOXYCARBONYLAMINO-PHENYL-ACETIC ACID Chemical Properties

Melting point:
111-112℃
Boiling point:
407.2±38.0 °C(Predicted)
Density 
1.182±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
Solid
pka
3.51±0.10(Predicted)
color 
White to off-white
optical activity
Consistent with structure
CAS DataBase Reference
3601-66-9(CAS DataBase Reference)
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TERT-BUTOXYCARBONYLAMINO-PHENYL-ACETIC ACID Usage And Synthesis

Uses

Boc-DL-Phg-OH is a Glycine.html" class="link-product" target="_blank">Glycine (HY-Y0966) derivative[1].

Synthesis

24424-99-5

2835-06-5

2900-27-8

General procedure for the synthesis of BOC-L-phenylglycine from di-tert-butyl dicarbonate and 2-amino-2-phenylacetic acid: DL-2-phenylglycine (5.0 g, 33 mmol) was dissolved in 1 N NaOH solution (132 mL). Subsequently, di-tert-butyl dicarbonate (19.0 mL, 82.7 mmol) was added and the reaction mixture was stirred at room temperature until the reaction was complete. N-tert-butoxycarbonyl-DL-phenylglycine was isolated as a white solid (7.61 g, 92% yield) by appropriate post-processing steps.

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

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