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Chemical Structure| 30924-93-7 Chemical Structure| 30924-93-7
Chemical Structure| 30924-93-7

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Boc-Ser(Bzl)-OH is a serine derivative, used for biochemical research and drug synthesis.

Synonyms: Boc-Glu-OBzl

4.5 *For Research Use Only !

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Product Details of Boc-Glu-OBzl

CAS No. :30924-93-7
Formula : C17H23NO6
M.W : 337.37
SMILES Code : O=C(O)CC[C@@H](C(OCC1=CC=CC=C1)=O)NC(OC(C)(C)C)=O
Synonyms :
Boc-Glu-OBzl
MDL No. :MFCD00065568
InChI Key :CVZUKWBYQQYBTF-ZDUSSCGKSA-N
Pubchem ID :153708

Safety of Boc-Glu-OBzl

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

Application In Synthesis of Boc-Glu-OBzl

* 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 [ 30924-93-7 ]

[ 30924-93-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 30924-93-7 ]
  • [ 29390-67-8 ]
  • 61-(N5-L-O1-benzyl-N2-tert-butoxycarbonyl-glutamino)-61-deoxycyclomaltoheptaose [ No CAS ]
  • 2
  • [ 30924-93-7 ]
  • [ 29390-67-8 ]
  • [ 197576-60-6 ]
YieldReaction ConditionsOperation in experiment
86% Compound 7 (0.337 g, 1.0 mmol), HOBT (0.135 g, 1.0 mmol) and DCC (0.206 g, 1.0 mmol), were dissolved in DMF (5 ml) and stirred at 25° C. for 1 h. Compound 4 (1.134 g, 1.0 mmol) was added and the stirring was continued for 24 h at 25° C. Then, the precipitate was filtered and the DMF was removed by evaporation under reduced pressure. The residue was triturated with hot acetone (100 ml), and the precipitate was filtered and dried under vacuum. The product was recrystallized from hot water yielding 1.25 g (86percent yield) of 6 as a white crystalline solid. TLC analysis of 6 performed on silica plates (EtOAc:2-propanol:conc. NH4OH:water-7:7:5:4) showed one major spot (Rf=0.56). 1H NMR (DMSO-d6) delta: 1.35 (s, 9H), 1.6-2.2 (m, 4H), 3.30-3.65 (m, 42H), 4.45 (m, 6H), 4.85 (m, 7H), 5.1 (s, 2H), 5.62-5.78 (m, 14H), 7.35 (s, 5H). HPLC (Luna 5u NH2 100 A, size 250-4.6 mm, mobile phase 65percent acetonitrile-35percent H2O, flow 1.2 ml/min), Rt=5.8 min.
With dmap; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 25℃; for 25h;Product distribution / selectivity; Compound 7 (0.337 g, 1.0 mmol) and DCC (0.206 g, 1.0 mmol) were dissolved in DMF (5 ml) and stirred at 25° C. for 1 h. Compound 4 (1.134 g, 1.0 mmol) and (DMAP, 0.122 g, 1.0 mmol) were added and the stirring was continued for 24 h at 25° C. The reaction work-up, isolation of the product, and TLC and 1H NMR data are as described in Example 6.
Compound 7 (0.337 g, 1.0 mmol), HOBT (0.135 g, 1.0 mmol), and DCC (0.206 g, 1.0 mmol) were dissolved in DMF (5 ml) and stirred at 25° C. for 1 h. Compound 4 (1.134 g, 1.0 mmol) and dry zeolite Na-X (0.5 g) were added and the stirring was continued for 24 h at 25° C. The reaction work-up, isolation of the product and TLC and 1H NMR data are as described in Example 6 above.
  • 3
  • [ 30924-93-7 ]
  • [ 486460-21-3 ]
  • C23H28F3N5O5 [ No CAS ]
  • 4
  • [ 30924-93-7 ]
  • [ 91229-86-6 ]
 

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