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Chemical Structure| 173963-91-2 Chemical Structure| 173963-91-2

Structure of Fmoc-L-Cys(Boc-aminopropyl)-OH
CAS No.: 173963-91-2

Chemical Structure| 173963-91-2

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Product Details of [ 173963-91-2 ]

CAS No. :173963-91-2
Formula : C26H32N2O6S
M.W : 500.61
SMILES Code : CC(C)(C)OC(NCCCSC[C@@H](C(O)=O)NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)=O
MDL No. :MFCD01318742
InChI Key :VODQCWHZYBQNRK-QFIPXVFZSA-N
Pubchem ID :18392904

Safety of [ 173963-91-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 173963-91-2 ]

* 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 [ 173963-91-2 ]

[ 173963-91-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 82911-69-1 ]
  • (R)-2-Amino-3-(3-tert-butoxycarbonylamino-propylsulfanyl)-propionic acid [ No CAS ]
  • [ 173963-91-2 ]
  • 2
  • [ 24424-99-5 ]
  • [ 173963-91-2 ]
  • 3
  • [ 83948-53-2 ]
  • [ 173963-91-2 ]
  • 4
  • [ 173963-91-2 ]
  • S-(3-aminopropyl)-Nα-Fmoc-L-cysteine [ No CAS ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid; In dichloromethane; at 20.0℃; for 0.416667h; 2.5 g (5 mmol) S-(Nw-Boc-3-aminoethyl)-Na-Fmoc-L-cysteine was dissolved in 25 mL dichloromethane and deprotected by the addition of 8 mL trifluoroacetic acid with 25 minutes stirring at room temperature. The solvent was evaporated in vacuo to afford S-(3-aminoethyl)-Na-Fmoc-L-cysteine.
 

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