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[ CAS No. 134471-24-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 134471-24-2
Chemical Structure| 134471-24-2
Structure of 134471-24-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 134471-24-2 ]

CAS No. :134471-24-2 MDL No. :MFCD00037568
Formula : C14H9NO7 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 303.22 Pubchem ID :-
Synonyms :
7-Hydroxycoumarin-3-carboxylic acid N-succinimidyl ester
Chemical Name :2,5-Dioxopyrrolidin-1-yl 7-hydroxy-2-oxo-2H-chromene-3-carboxylate

Safety of [ 134471-24-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 134471-24-2 ]

* 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 [ 134471-24-2 ]

[ 134471-24-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 33921-17-4 ]
  • [ 134471-24-2 ]
  • [ 848332-04-7 ]
YieldReaction ConditionsOperation in experiment
20.3 mg In N,N-dimethyl-formamide at 20℃; for 3h;
  • 2
  • [ 66-84-2 ]
  • 2,5-dioxopyrrolidin-1-yl 7-hydroxy-2-oxo-2H-chromene-3-carboxylate [ No CAS ]
  • 2-deoxy-2-((7-hydroxycoumarin-3-yl) carboxamido)-D-glucose [ No CAS ]
YieldReaction ConditionsOperation in experiment
44% With triethylamine; In water; N,N-dimethyl-formamide; at 20℃; for 3h;Cooling with ice; Synthesis of 2-HCDG (2-Deoxy-2-((7-hydroxycoumarin-3-yl) carboxamido)-D-glucose) (0185) 2-HCDG represented by the following formula was synthesized as described below. (0186) <strong>[66-84-2]D-glucosamine hydrochloride</strong> (11.9 mg) was dissolved in water (2 mL), and the solution was cooled with ice. To this was added triethylamine (9.2 muL), subsequently, 7-Hydroxycoumarin-3-carboxylic acid N-succinimidyl ester (20 mg) and dimethylformamide (2 mL) were added, and the mixture was stirred at room temperature for 3 hours. A 1% acetic acid aqueous solution (4 mL) was added and the solution was allowed to stand still overnight. The solution was allowed to pass through a membrane filter, and washed with a 1% acetic acid aqueous solution. The filtrate and the washing solution were combined and purified by HPLC. The intended fractions were collected and freeze dried. (0187) Yielded amount: 10.6 mg (0188) Yielded: 44% (0189) 1H-NMR (400 MHz, deuterated water, ppm): (0190) delta8.58 (s×2, 1H, Ar), delta7.53-delta7.56 (m, 1H, Ar), delta6.79 (m, 1H, Ar), delta6.67 (m, 1H, Ar), delta5.24 (d, 0.7H, J=3.7 Hz, H-1alpha), delta4.84 (d, 0.3H, J=8.2 Hz, H-1beta), delta3.41-delta4.06 (m, 6H, H-2, H-3, H-4, H-5, H-6, H-6). (0191) ESI-MS: calcd for C16H18NO9 [M+H]+ 368.10. found 368.1. (0192) Maximum excitation wavelength: 402 nm (0193) Maximum emission wavelength: 447 nm
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