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Chemical Structure| 54-86-4 Chemical Structure| 54-86-4

Structure of 54-86-4

Chemical Structure| 54-86-4

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Product Details of [ 54-86-4 ]

CAS No. :54-86-4
Formula : C6H4NNaO2
M.W : 145.09
SMILES Code : O=C(C1=CC=CN=C1)[O-].[Na+]
MDL No. :MFCD00064352

Safety of [ 54-86-4 ]

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

Application In Synthesis of [ 54-86-4 ]

* 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 [ 54-86-4 ]

[ 54-86-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 60372-77-2 ]
  • [ 54-86-4 ]
  • C20H40N4O3*C6H5NO2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
7.6 g In water; at 90℃; for 2h; Sodium niacin (purchased from Tishike (Shanghai) Chemical Industry Development Co., Ltd.) 2.0 g was dissolved in 50 mL of water to prepare a sodium nicotinate aqueous solution (A); 6.8 g of <strong>[60372-77-2]lauroyl arginine ethyl ester hydrochloride</strong> Dissolve in 40mL of water and heat to 90 C until the <strong>[60372-77-2]lauroyl arginine ethyl ester hydrochloride</strong> is completely dissolved to prepare an aqueous solution of <strong>[60372-77-2]lauroyl arginine ethyl ester hydrochloride</strong> (B); The saline solution (A) was slowly added to the <strong>[60372-77-2]lauroyl arginine ethyl ester hydrochloride</strong> aqueous solution (B), continuously stirred, reacted for 2 hours, cooled to room temperature, filtered, the precipitate was fully washed with purified water, and the precipitate was dried under vacuum at 60 C. That is, 7.6 g of a niacin ion pair compound was obtained.
 

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