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Boc-N-Me-Tyr-OH

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Boc-N-Me-Tyr-OH manufacturers

  • BOC-N-ME-TYR-OH
  • BOC-N-ME-TYR-OH pictures
  • $15.00
  • 2021-08-12
  • CAS:82038-34-4
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • BOC-N-ME-TYR-OH
  • 	BOC-N-ME-TYR-OH pictures
  • $7.00
  • 2019-09-02
  • CAS:82038-34-4
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 100KG
Boc-N-Me-Tyr-OH Basic information
Product Name:Boc-N-Me-Tyr-OH
Synonyms:BOC-N-Methyl-L-tyrosine;N-tert-Butoxycarbonyl-N-methyl-L-tyrosine;(S)-2-((tert-butoxycarbonyl)(Methyl)aMino)-3-(4-hydroxyphenyl)propanoic acid;Boc-N-Me-L-Tyr-OH;N-Boc-N-methyl-L-tyrosine;Boc-MeTyr-OH;N-[(1,1-DiMethylethoxy)carbonyl]-N-Methyl-L-tyrosine;L-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-
CAS:82038-34-4
MF:C15H21NO5
MW:295.33
EINECS:
Product Categories:Amino Acids & Derivatives;Aromatics;Tyrosine [Tyr, Y];Chiral Reagents
Mol File:82038-34-4.mol
Boc-N-Me-Tyr-OH Structure
Boc-N-Me-Tyr-OH Chemical Properties
Melting point 140-142℃
density 1.220
storage temp. 2-8°C
solubility soluble in Ethyl Acetate, Methanol
form Oil
color Colourless
CAS DataBase Reference82038-34-4(CAS DataBase Reference)
Safety Information
MSDS Information
Boc-N-Me-Tyr-OH Usage And Synthesis
Chemical PropertiesColourless Oil
UsesBOC-N-ME-TYR-OH is used in the preparation of tyrosyl derivatives as P2X7 receptor modulators.
Synthesis
O-TERT-BUTYLDIMETHYLSILYL-N-METHYL-N-T-BUTOXYCARBONYL-L-TYROSINE, METHYL ESTER

112196-58-4

BOC-N-ME-TYR-OH

82038-34-4

Methyl (S)-2-((tert-butoxycarbonyl)(methyl)amino)-3-(4-((tert-butyldimethylsilyl)oxy)phenyl)propionate (57) (4.0 g, 9.44 mmol) was used as a raw material, which was dissolved in a mixed solvent of THF:MeOH:H2O (3:1:1, 14.4 mL:4.8 mL:4.8 mL). LiOH-H2O (0.714 g, 17.02 mmol) was added to this solution at 0 °C. The reaction mixture was stirred at the same temperature for 1 h. LCMS monitoring showed complete consumption of the feedstock. After completion of the reaction, the reaction mixture was diluted with water (40 mL) and ethyl acetate (50 mL). The aqueous layer was acidified to pH 4-5 with 5% citric acid solution and subsequently extracted with ethyl acetate (2 x 100 mL). The organic layers were combined, dried over sodium sulfate, and concentrated under reduced pressure to afford (S)-2-((tert-butoxycarbonyl)(methyl)amino)-3-(4-hydroxyphenyl)propanoic acid (58) (2.78 g, 9.4 mmol, 100% yield) as a slightly reddish oil, which could be used for the next step of the reaction without further purification.MS (ESI): 294.2, [M-1]-.

References[1] Tetrahedron Letters, 2018, p. 4267 - 4271
[2] Journal of Organic Chemistry, 1988, vol. 53, # 3, p. 487 - 499
Tag:Boc-N-Me-Tyr-OH(82038-34-4) Related Product Information
Boc-N-alpha-methyl-O-benzyl-L-tyrosine Boc-N-methyl-L-phenylalanine BOC-N-methyl-D-alanine Boc-N-Methyl-L-phenylglycine N-tert-Butyloxycarbonyl-N-methyl-O-benzyl-L-threonine Boc-7-hydroxy-Tic-OH Boc-N-Me-Tyr-OH Boc-3-amino-L-tyrosine Boc-3-iodo-L-tyrosine Boc-[15N]Tyr-OH Boc-3-nitro-L-tyrosine Boc-N-Me-Tyr-OH Boc-N-Me-Tyr(Ac)-OH dcha Boc-MeTyr(Me)-OH dcha Boc-N-Me-Tyr(2,6-dichloro-Bzl)-OH O-tert-Butyldimethylsilyl-N-methyl-N-t-butoxycarbonyl-L-tyrosine, methyl ester Boc-D-O-Tyr-OH, Boc-L-m-Tyr-OH,