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Chemical Structure| 3507-28-6 Chemical Structure| 3507-28-6

Structure of 3507-28-6

Chemical Structure| 3507-28-6

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Product Details of [ 3507-28-6 ]

CAS No. :3507-28-6
Formula : C8H6ClNOS
M.W : 199.66
SMILES Code : COC1=CC2=C(SC(Cl)=N2)C=C1
MDL No. :MFCD00160069
InChI Key :UUERHMFUYYXLRE-UHFFFAOYSA-N
Pubchem ID :7059200

Safety of [ 3507-28-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 3507-28-6 ]

* 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 [ 3507-28-6 ]

[ 3507-28-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 55690-60-3 ]
  • [ 3507-28-6 ]
YieldReaction ConditionsOperation in experiment
20% With sulfuryl dichloride; In tetrahydrofuran; Sulfuryl chloride (1.64 mL) was added to a solution of 5-methoxy-2- mercaptobenzothiazole in THF (20 mL). After stirring overnight, ice water was added. The reaction mixture was allowed to warm to rt and was diluted with EtOAc (100 mL). This was washed with water (50 mL) and brine (50 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The material was purified by column chromatography (0 to 3% EtOAc in hexanes gradient), yielding 0.407 g (20%) of the title compound as a white solid. LC-MS: RT = 9.05 min., [M+H]+ = 2O0.0. R/= 0.38 in 10% EtOAc/Hexanes.
A mixture of 5-methoxy-1,3-benzothiazole-2-thiol (500 mg), thionyl chloride (2 mL) and DMF (1 drop) was stirred at 50 C. for 3 days. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture, and the obtained mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (211 mg).1H NMR (300 MHz, DMSO-d6) δ 3.84 (3H, s), 7.15 (1H, dd, J=9.0, 2.5 Hz), 7.53 (1H, d, J=2.5 Hz), 7.97 (1H, d, J=9.0 Hz).
 

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