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Chemical Structure| 6903-79-3 Chemical Structure| 6903-79-3
Chemical Structure| 6903-79-3

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Aplodan is a molecule with anti-ischemia and anti-arrhythmic activities that can protect cell membranes, aiding research on ischemic heart disease or ischemic heart disease accompanied by persistent ventricular premature beats (VPB).

Synonyms: Creatinol O-phosphate; Creatinol phosphate; Creatinolfosfate, Creatinol Phosphate

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of Aplodan

CAS No. :6903-79-3
Formula : C4H12N3O4P
M.W : 197.13
SMILES Code : NC(N(C)CCOP(O)(O)=O)=N
Synonyms :
Creatinol O-phosphate; Creatinol phosphate; Creatinolfosfate, Creatinol Phosphate
English Name :2-(1-Methylguanidino)ethyl dihydrogen phosphate
MDL No. :MFCD00868297
InChI Key :FOIPWTMKYXWFGC-UHFFFAOYSA-N
Pubchem ID :23342

Safety of Aplodan

Application In Synthesis of Aplodan

* 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 [ 6903-79-3 ]

[ 6903-79-3 ] Synthesis Path-Downstream   1~4

YieldReaction ConditionsOperation in experiment
Hydrolyse (Fig.2);
YieldReaction ConditionsOperation in experiment
Creatinol*HBr, POCl3,H2O;
Creatinol 1)H3PO4 2)Dehydratisierung(165grad);
Creatinol-N-phosphat (II), 155grad;
Kreatinol-phosphat, Polyphosphorsaeure;
Guanidin II, Chlorphosphorsaeure;
Creatinolo N-fosfato, 155grad, 1 Std.;
Creatinol , H3PO4;
aus 2-<Carbimidoyl-methyl-amino>-ethanol('Kreatinol')-hydrobromid und Phosphoroxychlorid in W.;

  • 3
  • [ 1296150-88-3 ]
  • [ 6903-79-3 ]
YieldReaction ConditionsOperation in experiment
With water at 90℃; for 5h; 1 Example 1 In the reaction flask volume 1000ml concentrated phosphoric acid was added 75g (0.65mol), phosphorous pentoxide was added in 66g (0.46mol), was added when the reaction temperature is controlled at 60 ~ 110 ° C, holding for 1 hour; added muscle alcohol phosphate 30g (0.14mol), 80 ° C reaction was stirred for 5 hours; water was added 20g (l 1 lmol.), incubation was continued for 5 hours; 90 ° C the reaction was concentrated under reduced pressure to no distillate, the solvent was added and stirred until the precipitate has, stirring continued for 5 hours; the reaction was filtered off with suction, the filter cake was obtained, 80 ° C and dried to a constant weight, yield about 80%, the product IR, 13C spectrum see Fig.
  • 4
  • [ 6903-79-3 ]
  • [ 2719727-11-2 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With dmap; triethylamine In tetrahydrofuran 1.6 Step 6: The unprotected hydroxyl group of intermediate 5 reacts with inositol phosphate to obtain intermediate 6
 

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