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BOC-D-TYR(ME)-OH

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CAS:68856-96-2
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CAS:68856-96-2
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CAS:68856-96-2
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Products Intro: Product Name:BOC-D-TYR(ME)-OH
CAS:68856-96-2
Purity:98% Package:1kg,5kg,10kg

BOC-D-TYR(ME)-OH manufacturers

  • Boc-D-Tyr(me)-OH
  • Boc-D-Tyr(me)-OH pictures
  • $0.00 / 1kg
  • 2026-05-14
  • CAS:68856-96-2
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
BOC-D-TYR(ME)-OH Basic information
Product Name:BOC-D-TYR(ME)-OH
Synonyms:(R)-2-TERT-BUTOXYCARBONYLAMINO-3-(4-METHOXY-PHENYL)-PROPIONIC ACID;N-ALPHA-T-BUTOXYCARBONYL-4-METHOXY-D-PHENYLALANINE;(2R)-3-(4-methoxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid;Boc-O-methyl-D-tyrosine≥ 98% (HPLC);Boc-π-methoxy-D-Phe-OH;N-ALPHA-T-BOC-O-METHYL-D-TYROSINE;N-ALPHA-T-BOC-P-METHOXY-D-PHENYLALANINE;N-ALPHA-T-BUTOXYCARBONYL-O-METHYL-D-TYROSINE
CAS:68856-96-2
MF:C15H21NO5
MW:295.33
EINECS:
Product Categories:Unusual Amino Acids;Boc-Amino Acids and Derivative
Mol File:68856-96-2.mol
BOC-D-TYR(ME)-OH Structure
BOC-D-TYR(ME)-OH Chemical Properties
Melting point 93.0 to 97.0 °C
Boiling point 462.0±40.0 °C(Predicted)
density 1.168±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
pka3.00±0.10(Predicted)
form powder to crystal
color White to Almost white
Optical RotationConsistent with structure
Safety Information
HazardClass IRRITANT
HS Code 2924297099
MSDS Information
BOC-D-TYR(ME)-OH Usage And Synthesis
Chemical PropertiesWhite powder
UsesBoc-O-methyl-D-tyrosine is a compound involved in the design and synthesis of β-sheet-based self-assembling cyclic peptides with tunable cavities.
Synthesis
oc-O-Methyl-L-TyrosineMethylEster

94790-24-6

BOC-D-TYR(ME)-OH

68856-96-2

General procedure for the synthesis of N-Boc-4-methoxy-D-phenylalanine from methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(4-methoxyphenyl)propionate: in the presence of 1 mL of water, K2CO3 (0.089 g, 0.608 mmol) was added to a (S)-2-((tert-butoxycarbonyl)amino)-3-(4-methoxyphenyl) Methyl propionate (0.100 g, 0.323 mmol) was added to a solution in methanol (4 mL). The reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, methanol was removed by rotary evaporation. The reaction mixture was diluted with water and the aqueous layer was extracted with ethyl acetate. The organic layers were combined, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography using ethyl acetate and petroleum ether (1:1) as eluent to give pure N-Boc-4-methoxy-D-phenylalanine.

References[1] Tetrahedron Letters, 2012, vol. 53, # 52, p. 7128 - 7130
[2] Journal of Organic Chemistry, 1981, vol. 46, # 9, p. 1944 - 1946
[3] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 19, p. 5607 - 5612
BOC-D-TYR(ME)-OH Preparation Products And Raw materials
Raw materialsoc-O-Methyl-L-TyrosineMethylEster-->Potassium carbonate-->Methanol-->Water
Tag:BOC-D-TYR(ME)-OH(68856-96-2) Related Product Information
BOC-D-TYR(ET)-OH BOC-D-TYR(BZL)-OH N-tert-Butyloxycarbonyl-O-(2-bromobenzyloxycarbonyl)-D-tyrosine Boc-Tyr(Me)-OH BOC-L-TYR(BZL)-OH Boc-L-Tyr(tBu)-OH O-METHYL-D-TYROSINE Boc-D-Tyr-OH BOC-D-TYR(BZL)-OSU BOC-D-TYR(2,6-DI-CL-BZL)-OH BOC-D-TYR(ALL)-OH,BOC-D-TYR(AL)-OH BOC-D-TYR(BZL, 3-NO2)-OH BOC-D-3,4-DIMETHOXYPHENYLALANINE BOC-D-METYR(BZL)-OH CHA BOC-D-TYR(ME)-OH Boc-D-Tyr(tBu)-OH BOC-BETA-TYR(ME)-OH BOC-L-TYR(BOC)-OH