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Chemical Structure| 126826-36-6 Chemical Structure| 126826-36-6

Structure of 126826-36-6

Chemical Structure| 126826-36-6

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Product Details of [ 126826-36-6 ]

CAS No. :126826-36-6
Formula : C5H4Br2N2S
M.W : 283.97
SMILES Code : CSC1=NC(Br)=CC(Br)=N1
MDL No. :MFCD27951946

Safety of [ 126826-36-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 126826-36-6 ]

* 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 [ 126826-36-6 ]

[ 126826-36-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1979-98-2 ]
  • [ 126826-36-6 ]
YieldReaction ConditionsOperation in experiment
73% With phosphorus(V) oxybromide; In acetonitrile; 4,6-Dihydroxy-2-methylthiopyrimidine (27 g; European Patent Application No. 0343752) was added portionwise to a mixture of phosphoryl bromide (196 g) and acetonitrile (500 ml). The mixture was stirred and heated to reflux for 3 hours. The mixture was evaporated and the residue was poured onto ice and extracted with diethyl ether. The organic phase was dried (MgSO4) and evaporated. The residue was purified by column chromatography using a 97:3 mixture of petroleum ether and ethyl acetate as eluent. There was thus obtained 4,6-dibromo-2-methylthiopyrimidine (35 g, 73%).
  • 2
  • [ 1979-98-2 ]
  • [ 7789-59-5 ]
  • [ 126826-36-6 ]
YieldReaction ConditionsOperation in experiment
In ethyl acetate; (1) Synthesis of an intermediate, 4,6-dibromo-2-(methylthio)pyrimidine (Compound IV-3) Into a 300 ml eggplant type flask, 4,6-dihydroxy-2-(methylthio)pyrimidine (Compound IV-124) (12.5 g, 0.079 mol) and phosphoryl tribromide (49.8 g, 0.079*2.1 mol) were introduced, and the flask was immersed in 80 C. oil bath and the solution was stirred for 30 minutes. The reaction mixture was cooled to room temperature, then ethyl acetate was added thereto and dissolved. The resulting solution was poured onto ice and an organic phase was separated. The separated organic phase was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate and filtered, and thereafter, the solvent was distilled off. The residue was purified on silica gel column chromatography (Wakogel C300, 300 ml, ethyl acetate/hexane=35 ml/700 ml) to obtain the compound (IV-3) as a white crystalline product from the fraction of 20 ml to 480 ml. Yield: 14.6 g. m.p. 90 to 92 C.
In ethyl acetate; (1) Synthesis of an intermediate, 4,6-dibromo-2-(methylthio)pyrimidine (Compound No. VII-22) Into a 300 ml eggplant type flask, 4,6-dihydroxy-2-(methylthio)pyrimidine (12.5 g, 0.079 mol) and phosphoryl tribromide (49.8 g, 0.079*2.1 mol) were introduced and the flask was immersed in an 80 C. oil bath, and the mixture was then stirred for 30 minutes. The reaction mixture was allowed to cool to room temperature and dissolved in ethyl acetate, and then poured onto ice to separate an organic phase. The organic phase was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and filtered, and thereafter the solvent was distilled off. The residue was purified on silica gel column chromatography (Wakogel C300, 300 ml, ethyl acetate/hexane=35 ml/700 ml) to obtain a white crystal from the fraction of 120 ml to 480 ml. Yield: 14.6 g. Melting point: 90-92 C.
 

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