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Chemical Structure| 1095823-35-0 Chemical Structure| 1095823-35-0

Structure of 1095823-35-0

Chemical Structure| 1095823-35-0

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Product Details of [ 1095823-35-0 ]

CAS No. :1095823-35-0
Formula : C15H16N2O4S
M.W : 320.36
SMILES Code : O=C(C1=CN=C(CNC(OCC2=CC=CC=C2)=O)S1)OCC
MDL No. :MFCD23159416

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Application In Synthesis of [ 1095823-35-0 ]

* 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 [ 1095823-35-0 ]

[ 1095823-35-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 49548-40-5 ]
  • [ 33142-21-1 ]
  • [ 1095823-35-0 ]
YieldReaction ConditionsOperation in experiment
19% In N,N-dimethyl-formamide; at 50℃; for 72h; Synthesis of Compound A.4. To a solution of aldehyde A.3 (54 g, 0.36 mol) in anhydrous DMF (42 mL), was added a solution of compound A.2 (40.3 g, 0.18 mol) in anhydrous DMF (320 mL). The reaction was heated at 50 C. for 3 days. The mixture was cooled to 0 C., and Et2O (390 mL) followed by sat. NaHCO3 solution (200 mL) were added slowly. After separation of the phases, the aqueous layer was extracted with Et2O (2×300 mL). The combined organic extracts were washed with sat. NaHCO3 (3×500 mL), dried (Na2SO4) and concentrated under reduced pressure to give crude material as thick brown oil, which was purified by column chromatography (EtOAc/hexanes) to give compound A.4 as a brown solid (22 g, 19%). 1H NMR: (CDCl3, 200 MHz) delta: 8.3 (s, 1H), 7.4 (s, 5H), 5.6 (brs, 1H), 5.2 (s, 2H), 4.7 (d, 2H, J=5 Hz), 4.4 (m, 2H), 1.4 (m, 3H); MS: m/z 320.9 [M+1]+.
19% To a solution of aldehyde A.3 (54 g, 0.36 mol) in anhydrous DMF (42 mL), was added a solution of compound A.2 (40.3 g, 0.18 mol) in anhydrous DMF (320 mL). The reaction was heated at 50 C. for 3 days. The mixture was cooled to 0 C., and Et2O (390 mL) followed by sat. NaHCO3 solution (200 mL) were added slowly. After separation of the phases, the aqueous layer was extracted with Et2O (2×300 mL). The combined organic extracts were washed with sat. NaHCO3 (3×500 mL), dried (Na2SO4) and concentrated under reduced pressure to give crude material as thick brown oil, which was purified by column chromatography (EtOAc/hexanes) to give compound A.4 as a brown solid (22 g, 19%). 1H NMR: (CDCl3, 200 MHz) delta: 8.3 (s, 1 H), 7.4 (s, 5 H), 5.6 (brs, 1 H), 5.2 (s, 2H), 4.7 (d, 2 H, J=5 Hz), 4.4 (m, 2 H), 1.4 (m, 3 H); LCMS: m/z 320.9 [M+1]+.
  • 2
  • C11H13NO2S2 [ No CAS ]
  • [ 33142-21-1 ]
  • [ 1095823-35-0 ]
YieldReaction ConditionsOperation in experiment
19% In N,N-dimethyl-formamide; at 50℃; for 72h; To a solution of aldehyde G.2 (54 g, 0.36 mol) in anhydrous DMF (42 mL), was added a solution of compound G.I (40.3 g, 0.18 mol) in anhydrous DMF (320 mL). The reaction was heated at 50 C for 3 days. The mixture was cooled to OC, and Et2O (390 mL) followed by sat. NaHCO3 solution (200 mL) were added slowly. After separation of the phases, the aqueous layer was extracted with Et2O (2 x 300 mL). The combined organic extracts were washed with sat. NaHCO3 (3 x 500 mL), dried (Na2SO^ and concentrated under reduced pressure to give crude material as thick brown oil, which was purified by column chromatography (EtOAc/hexanes) to give compound G.3 as a brown solid (22 g, 19 %). 1B NMR: (CDCl3, 200 MHz) delta 8.3 (s, 1H), 7.4 (s, 5H), 5.6 (brs, 1H), 5.2 (s, 2H), 4.7 (d, 2 H, J = 5 Hz), 4.4 (m, 2H), 1.4 (m, 3H); LCMS: m/z 320.9 [M+l].
 

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