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Chemical Structure| 60166-86-1 Chemical Structure| 60166-86-1

Structure of 60166-86-1

Chemical Structure| 60166-86-1

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Product Details of [ 60166-86-1 ]

CAS No. :60166-86-1
Formula : C6H6O4S2
M.W : 206.24
SMILES Code : CS(=O)(=O)C1=CC=C(S1)C(O)=O
MDL No. :MFCD00173745
InChI Key :SLWRTVINHWIGTK-UHFFFAOYSA-N
Pubchem ID :2740497

Safety of [ 60166-86-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of [ 60166-86-1 ]

* 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 [ 60166-86-1 ]

[ 60166-86-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 114365-04-7 ]
  • [ 60166-86-1 ]
  • 5-(methylsulfonyl)-N-(4-(pyrrolidin-1-yl)benzyl)thiophene-2-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
20% With N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane; at 0℃; for 1h; To a stirred reaction mixture of 5-methylsulfonylthiophene-2-carboxylic acid (200 mg, 0.9697 mmol) and al2 (205.11 mg, 1.1637 mmol) in DCM (20 mL) was added HATU (553.09 g, 1.4546 mmol) followed by DIPEA (376.02 mg, 2.9092 mmol) at 0 C, then stirring was continued further for 1 h at 0 C. The reaction mixture was concentrated under reduced pressure, and then diluted by adding water (10.0 mL) and then the reaction mixture was extracted with EtOAc (2x25 mL), the combined extracts were dried over anhydrous Na2SC>4, filtered, concentrated under reduced pressure to obtain the crude residue (220 mg) as a viscous liquid. The crude material was purified by Combi-Flash column chromatography (100-200 silica gel), eluting 0-40% EtOAc in hexanes to afford 23 (75.4 mg, 0.2012 mmol, 20% yield) as a solid. LCMS: 365.1 (M+H), Rt = 2.206 min, Column: X-Bridge BEH C- 18(3.0X50mm, 2.5pm); Mobile Phase: A: 0.025% FA in Water, B: ACN; (0302) T/B%:0.01/2, 0.2/2, 2/98, 3/98, 3.2/2, 4/2; Flow rate: 1.2ml/min (Gradient); Column Oven temperature: 50 C. HPLC: Rt= 6.138 min, 97.26%; Column: XSELECT CSH C18 (150 X 4.6mm, 3.5p); Mobile Phase-A:0.05%TFA: ACETONITRILE (95:05); Mobile Phase- B: ACETONITRILE :0.05%TFA(95:05); Program:T/B%: 0.01/10,12/90,16/90; Flow : 1.0 mL/min; Diluent -de) d 9.23 (t, 1H), 7.84 (d, 1H), 7.79 (d, 1H), 7.11 (d, 2H), 6.49 (d, 2H), 4.33 (d, 2H), 3.37 (s, 3H), 3.18 (t, 4H), 1.98 - 1.89 (m, 4H).
20% With N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane; at 0℃; for 1h; To a stirred reaction mixture of 5-methylsulfonylthiophene-2-carboxylic acid (200 mg, 0.9697 mmol) and al2 (205.11 mg, 1.1637 mmol) in DCM (20 mL) was added HATU (553.09 g, 1.4546 mmol) followed by DIPEA (376.02 mg, 2.9092 mmol) at 0 C, then stirring was continued further for 1 h at 0 C. The reaction mixture was concentrated under reduced pressure, and then diluted by adding water (10.0 mL) and then the reaction mixture was extracted with EtOAc (2x25 mL), the combined extracts were dried over anhydrous Na2SC>4, filtered, concentrated under reduced pressure to obtain the crude residue (220 mg) as a viscous liquid. The crude material was purified by Combi-Flash column chromatography (100-200 silica gel), eluting 0-40% EtOAc in hexanes to afford 23 (75.4 mg, 0.2012 mmol, 20% yield) as a solid. LCMS: 365.1 (M+H), Rt = 2.206 min, Column: X-Bridge BEH C- 18(3.0X50mm, 2.5pm); Mobile Phase: A: 0.025% FA in Water, B: ACN; (0302) T/B%:0.01/2, 0.2/2, 2/98, 3/98, 3.2/2, 4/2; Flow rate: 1.2ml/min (Gradient); Column Oven temperature: 50 C. HPLC: Rt= 6.138 min, 97.26%; Column: XSELECT CSH C18 (150 X 4.6mm, 3.5p); Mobile Phase-A:0.05%TFA: ACETONITRILE (95:05); Mobile Phase- B: ACETONITRILE :0.05%TFA(95:05); Program:T/B%: 0.01/10,12/90,16/90; Flow : 1.0 mL/min; Diluent -de) d 9.23 (t, 1H), 7.84 (d, 1H), 7.79 (d, 1H), 7.11 (d, 2H), 6.49 (d, 2H), 4.33 (d, 2H), 3.37 (s, 3H), 3.18 (t, 4H), 1.98 - 1.89 (m, 4H).
 

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