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Chemical Structure| 16977-78-9 Chemical Structure| 16977-78-9

Structure of 16977-78-9

Chemical Structure| 16977-78-9

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Product Details of [ 16977-78-9 ]

CAS No. :16977-78-9
Formula : C16H23BrO10
M.W : 455.25
SMILES Code : O=C(OC[C@@H](O1)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OCCBr)C
MDL No. :MFCD09840124

Safety of [ 16977-78-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 16977-78-9 ]

* 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 [ 16977-78-9 ]

[ 16977-78-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 295-64-7 ]
  • [ 16977-78-9 ]
  • acetic acid 3,5-diacetoxy-2-acetoxymethyl-6-[2-(1,4,7,10,13pentaaza-cyclopentadec-1-yl)-ethoxy]-tetrahydro-pyran-4-yl ester [ No CAS ]
  • 2
  • [ 21252-69-7 ]
  • [ 16977-78-9 ]
  • 1-octyl-3-[2-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)ethyl]imidazolium bromide [ No CAS ]
YieldReaction ConditionsOperation in experiment
95% In 5,5-dimethyl-1,3-cyclohexadiene; at 125℃; for 1h; General procedure: A solution of 2-bromoethyl glucoside 2 (1.1 mmol) and the alkylated imidazole 4 (3.3 mmol) in xylene (2 mL) was heated to 125 °C for 1 h. The solvent was evaporated and the crude product was taken up in MeCN (10 mL) and extracted 4 times with hexane (60 mL) to remove remaining imidazole 4. The acetonitrile phase was concentrated under reducing pressure to provide the desired product 5 as a pale yellow syrup in ~95percent yield.
  • 3
  • [ 21252-69-7 ]
  • [ 16977-78-9 ]
  • 1-(2-β-D-glucopyranosyloxyethyl)-3-octylimidazolium bromide [ No CAS ]
 

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