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Chemical Structure| 3417-91-2 Chemical Structure| 3417-91-2
Chemical Structure| 3417-91-2

H-Tyr-OMe·HCl

CAS No.: 3417-91-2

H-Tyr-OMe·HCl is a tyrosine derivative, commonly used in biochemical research and drug synthesis.

Synonyms: H-Tyr-OMe.HCl

4.5 *For Research Use Only !

Cat. No.: A137979 Purity: 98%

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Product Details of H-Tyr-OMe·HCl

CAS No. :3417-91-2
Formula : C10H14ClNO3
M.W : 231.68
SMILES Code : N[C@@H](CC1=CC=C(C=C1)O)C(OC)=O.[H]Cl
Synonyms :
H-Tyr-OMe.HCl
MDL No. :MFCD00012607

Safety of H-Tyr-OMe·HCl

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of H-Tyr-OMe·HCl

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 3417-91-2 ]

[ 3417-91-2 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 3417-91-2 ]
  • [ 4985-46-0 ]
YieldReaction ConditionsOperation in experiment
86% With ammonium hydroxide; at 20℃; for 4h; L-tyrosine methyl ester hydrochloride (1.16 g, 5 mmol) and concentrated aqueous ammonia (40 mL) were added to a 50 ml reaction vessel and stirred for 4 h at room temperature. Rotary evaporation of ammonia, spin dry, with anhydrous ethanol (20mL × 2) with water, column chromatography (silica gel, 200-300 mesh; exhibition Preparative, ethyl acetate: methanol: aqueous ammonia = 300: 10: 15) gave L-tyrosinamide in 86% yield.
  • 2
  • [ 3417-91-2 ]
  • [ 64205-12-5 ]
  • Z-D-Tyr-L-Tyr-OMe [ No CAS ]
  • 3
  • [ 20806-43-3 ]
  • [ 3417-91-2 ]
  • [ 105949-05-1 ]
  • 4
  • [ 3417-91-2 ]
  • [ 83345-46-4 ]
 

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