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[ CAS No. 14108-60-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 14108-60-2
Chemical Structure| 14108-60-2
Structure of 14108-60-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 14108-60-2 ]

CAS No. :14108-60-2 MDL No. :MFCD00070216
Formula : C13H13NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :JPZXHKDZASGCLU-UHFFFAOYSA-N
M.W : 215.25 Pubchem ID :250399
Synonyms :

Safety of [ 14108-60-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 14108-60-2 ]

* 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 [ 14108-60-2 ]

[ 14108-60-2 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 14108-60-2 ]
  • [ 6960-34-5 ]
  • [ 111726-64-8 ]
  • 3
  • [ 14108-60-2 ]
  • [ 76985-10-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: 76 percent / trifluoroacetic acid / a) 0 deg C, 2 h, b) RT, overnight 3: 95 percent / 2 N NaOH / ethanol / 37 °C 4: 90 percent
  • 4
  • [ 63-91-2 ]
  • [ 1197-17-7 ]
  • C20H36N3O7Pol [ No CAS ]
  • [ 14108-60-2 ]
  • C50H69N6O10Pol [ No CAS ]
YieldReaction ConditionsOperation in experiment
With 4-methyl-morpholine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; In N,N-dimethyl-formamide; for 1h; Then add the amino acids and other reagents required to add the side chain according to the peptide solid phase synthesis method. The molar ratio of amino acid feed is: Compound 4: amino acid: HBTU (benzotriazole-N, N, N ', N'-Tetramethyl Isourea hexafluorophosphate): NMM (N-methylmorpholine) = 1: 3: 2.85: 6. Connect 1-naphthylalanine in sequence according to the above method,4-aminomethylcyclohexanoic acid, phenylalanine,Add 3 equivalents of amino acid, add appropriate amount of DMF,Reaction for 1h. Transfer the synthetic product into a cutting tube,Add E solution, shake the cutting reaction for 1h; collect the cutting solution into a centrifuge tube, add 6 times the volume of ice ether,Precipitate on a low speed centrifuge; wash the precipitated crude product three times with ether to obtain the crude product of precursor compound 5.Purification by semi-preparative chromatography gave compound 5PSMA-Ala (Nap) -Cyh-Phe.
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