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Chemical Structure| 59795-47-0 Chemical Structure| 59795-47-0

Structure of 59795-47-0

Chemical Structure| 59795-47-0

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Product Details of [ 59795-47-0 ]

CAS No. :59795-47-0
Formula : C16H10O8
M.W : 330.25
SMILES Code : O=C(C1=CC=C(C(O)=O)C(C2=CC(C(O)=O)=CC=C2C(O)=O)=C1)O
MDL No. :N/A
InChI Key :BPFVHHLYBQRNKE-UHFFFAOYSA-N
Pubchem ID :18188463

Safety of [ 59795-47-0 ]

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

Application In Synthesis of [ 59795-47-0 ]

* 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 [ 59795-47-0 ]

[ 59795-47-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1004-38-2 ]
  • [ 59795-47-0 ]
  • 2C4H7N5*C16H10O8 [ No CAS ]
YieldReaction ConditionsOperation in experiment
69% In methanol; water; for 0.5h; General procedure: 2.2.1 Synthesis of [(C4H8N5+)·(C7H5O4-)]·2H2O hydrous salt (1) The <strong>[1004-38-2]TAP</strong>I (0.20 mmol) and HDHBA (0.40 mmol) were dissolved in 10 ml of methanol-distilled water (H2O) mixed solution. The mixed solution was stirred for 30 min to receive a colorless solution. After seven days of slow evaporation, crystals with good diffraction quality were obtained at 20-25 C. The resulting crystals were filtered and dried after rinsed with methanol-H2O mixed solution. Yield: 62%. Analysis calculated for C11H17N5O6: C, 41.85; H, 5.39; N, 22.20%. Found: C, 42.11; H, 5.42; N, 22.31%. Infrared spectrum (KBr disc, cm-1): 3429s, 3375s, 3315s, 3192s, 1683s, 1635s, 1610s, 1583s, 1516s, 1481m, 1424s, 1331m, 1303m, 1267m, 1245m, 1200w, 1163m, 1103w, 1007m, 982w, 940m, 920w, 853w, 871w, 797m, 767m, 730m, 698m, 665m, 470m.
 

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