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Chemical Structure| 31295-41-7 Chemical Structure| 31295-41-7

Structure of 31295-41-7

Chemical Structure| 31295-41-7

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Product Details of [ 31295-41-7 ]

CAS No. :31295-41-7
Formula : C4H6N4S2
M.W : 174.25
SMILES Code : NC1=C(N)C(S)=NC(S)=N1
MDL No. :MFCD00023229

Safety of [ 31295-41-7 ]

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

Application In Synthesis of [ 31295-41-7 ]

* 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 [ 31295-41-7 ]

[ 31295-41-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 121584-52-9 ]
  • [ 31295-41-7 ]
  • C64H109N15O12S2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
28.8% General procedure: A solution of <strong>[121584-52-9]acetyl-CsA-aldehyde</strong> (compound 1; 10 mg; 8 tmol) and 4,5-diamino-2,6-dimercaptopyrimidine (6.9 mg; 40 tmol) in MeOR (1 ml) was shacked at room temperature till completion of the reaction (control by analytical HPLC). Acetate hydrolysis, work-up of the reaction mixture and purification of the compound 16 were performed in the same manner as described for compound 14. Yield: 3.1 mg (28.8%); A solution of <strong>[121584-52-9]acetyl-CsA-aldehyde</strong> (compound 1; 20 mg)and tert-butyl-3-(3,4-diamino-phenyl)-acrylate (50 mg; 0.21mmol) in MeOH (1 ml) was shacked at room temperature tillcompletion of the reaction (control by analytical HPLC).The reaction mixture was cooled at 5 C., 0.2M NaOH (1ml) was added and the reaction mixture was shacked at 5C. till completion of the hydrolysis (control by analytical HPLC). Then, the reaction mixture was acidified with 18% chiorhydric acid (100 pi) and the product was purified by preparative HPLC. Yield: 5 mg (22.2%).
 

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