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Chemical Structure| 865813-91-8 Chemical Structure| 865813-91-8

Structure of 865813-91-8

Chemical Structure| 865813-91-8

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Product Details of [ 865813-91-8 ]

CAS No. :865813-91-8
Formula : C30H36N16O10
M.W : 780.71
SMILES Code : C[C@@]12[C@]3(N4C(N1CN5[C@@]6([H])N(C(N7[C@@]6([H])N(CN8[C@@]9([H])N(C(N%10[C@@]9([H])N(CN%11[C@]%12(N(C(N%13[C@]%12(N(COC%13)C%11=O)C)=O)C%10)C)C8=O)=O)C7)C5=O)=O)CN2C(N3COC4)=O)=O)C
MDL No. :N/A

Safety of [ 865813-91-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 865813-91-8 ]

* 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 [ 865813-91-8 ]

[ 865813-91-8 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 865813-91-8 ]
  • [ 540759-86-2 ]
  • [ 5471-84-1 ]
  • C52H60Br2N16O18S2(2-)*2Na(1+) [ No CAS ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid; at 70℃; for 3h; [0135] Dibromo dipropanesulfonate Host (figure 13). l,4-bis(2-bromoethoxy)benzene (250 mg, 0.768 mmol) and sodium 3,3'-(l,4-phenylenebis(oxy))bis(propane-l-sulfonate) (102 mg, 0.256 mmol) were added into a solution of methyl tetramer (200 mg, 0.256 mmol) in TFA (2.5 mL). The mixture was stirred and heated at 70 C for 3 h and then was poured into acetone (150 mL). The solid was collected by filtration. The crude solid was stirred with water (30 mL x 3) at RT for 4 hr. The filtrate was collected and the solvent was removed under reduced pressure. The producte was purified by recrystallization from H20 and MeOH (1: 1, 15 mL). The product was obtained as a white solid after drying under high vacuum (112 mg, 53%). 1H NMR (400 MHz, D20): 6.97 (s, 2H), 6.72 (s, 2H), 5.62 (d, J = 15.9, 2H), 5.60 (d, J = 15.9, 2H), 5.53 (d, J = 16.4, 2H), 5.45 (d, J = 5.8, 2H), 5.43 (d, J = 15.9, 2H), 5.40 (d, J = 5.0, 2H), 5.21 (d, J = 10.8, 2H), 4.27 (d, J = 16.4, 2H), 4.25-4.20 (m, 8H), 4.15-4.05 (m, 8H), 3.95-3.75 (m, 4H), 3.45-3.35 (m, 2H), 3.25-3.20 (m, 2H), 3.14 (t, J = 7.7, 4H), 2.35-2.15 (m, 4H), 1.87 (s, 3H), 1.81(s, 3H), 1.67 (s, 3H), 1.66 (s, 3H).
  • 2
  • [ 865813-91-8 ]
  • [ 5471-84-1 ]
  • C50H56Br4N16O12 [ No CAS ]
YieldReaction ConditionsOperation in experiment
79% With trifluoroacetic acid; at 70℃; for 3h; [0128] Tetrabromo Host (figure 9). l,4-bis(2-bromoethoxy)benzene (1.70 g, 5.21 mmol) and methyl tetramer (1.20 g, 1.53 mmol) were mixed in a round bottom flask. TFA (12 mL) was added, and the mixture was stirred at 70 C for 3 h. The reaction mixture was poured into MeOH (100 mL), and the solid was collected by filtration. The crude product was stirred with water (150 mL) and then acetone (150 mL) at RT and the solid was isolated by filtration. Drying at high vacuum gave the product as a white powder (1.71 g, 79 %). M.p. 283 - 285 C. IR (ATR, cm"1): 3000br, 1704m, 1456m, 1311m, 1225s, 1177s, 1080s, 966m, 922m, 818m, 794s, 754m, 666m. 1H NMR (400 MHz, DMSO): 6.91 (s, 4H), 5.59 (d, J =14.4, 2H), 5.51 (d, J = 15.2, 4H), 5.38 (d, J = 9.0, 2H), 5.30-5.25 (m, 6H), 4.50-4.40 (m, 4H), 4.25-4.20 (m, 10H), 4.06 (d, J = 15.2, 4H), 3.90-3.80 (m, 8H), 1.69 (s, 6H), 1.66 (s, 6H). 13C NMR (125 MHz, DMSO, 1,4-dioxane as internal reference): δ 156.0, 154.6, 151.0, 129.5,116.7, 78.0, 76.8, 71.5, 71.4, 71.0, 53.6, 48.9, 35.2, 33.5, 17.2, 16.3.
With acetic anhydride; trifluoroacetic acid; at 70℃; for 3h; Weigh 1.8 g (2.45 mmol) of the tetramer, add 8 mL of acetic anhydride and 8 mL of trifluoroacetic acid to the tetramer, Mix well in the oil bath at 70C. After the tetramer is completely dissolved, add 1.6 g (4.9 mmol) of the side arm of the bromobenzene ring to continue the reaction for 3 h
  • 3
  • [ 865813-91-8 ]
  • [ 5471-84-1 ]
  • C16H18O8S2(2-)*2Na(1+) [ No CAS ]
  • C56H62Br2N16O18S2(2-)*2Na(1+) [ No CAS ]
  • 4
  • [ 13794-15-5 ]
  • [ 865813-91-8 ]
  • sodium 3,3′-(1,4-phenylenebis(oxy))bis(propane-1-sulfonate) [ No CAS ]
  • C52H62N16O20S2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With acetic anhydride; trifluoroacetic acid; at 60℃; for 3.0h; Dissolve 1.8 g (2.45 mmol) of tetramer in 8 mL of acetic anhydride and 8 mL of trifluoroacetic acid,and mix wellunder oil bath conditions at 60 C.After the tetramer is completely dissolved, add two different The side arm of the benzene ring continues to react for 3 h;the molar ratio of thetetramer,the benzene ring side arm containing the sulfonic acid group, and the benzene ring side arm containing the carboxylic acid group is 1:1:1;.
 

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