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[ CAS No. 1129-25-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 1129-25-5
Chemical Structure| 1129-25-5
Structure of 1129-25-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1129-25-5 ]

CAS No. :1129-25-5 MDL No. :MFCD08752808
Formula : C7H7ClO2S2 Boiling Point : -
Linear Structure Formula :- InChI Key :ZCCHKGQZUSPUGJ-UHFFFAOYSA-N
M.W : 222.71 Pubchem ID :11138731
Synonyms :

Safety of [ 1129-25-5 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P301+P330+P331-P303+P361+P353-P304+P341-P305+P351+P338 UN#:3261
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1129-25-5 ]

* 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 [ 1129-25-5 ]

[ 1129-25-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 1129-25-5 ]
  • [ 82964-91-8 ]
YieldReaction ConditionsOperation in experiment
92% With dihydrogen peroxide In acetic anhydride; acetic acid
  • 2
  • [ 1129-25-5 ]
  • [ 264905-39-7 ]
  • [ 333987-42-1 ]
YieldReaction ConditionsOperation in experiment
With triethylamine In tetrahydrofuran; diethyl ether R.107.2 1-tert-Butoxycarbonyl-4-{ethyl[4-(methylsulfanyl)phenylsulfonyl]amino}piperidine REFERENCE EXAMPLE 107-2 1-tert-Butoxycarbonyl-4-{ethyl[4-(methylsulfanyl)phenylsulfonyl]amino}piperidine To a stirred solution of the title compound of reference example 107-1 (4.54 g, 19.9 mmol) in THF (50 mL) were added triethylamine (3.05 mL, 21.9 mmol) and 4-(methylsulfanyl)benzenesulfonyl chloride (4.42 g, 19.9 mmol) at 0° C., and the reaction mixture was stirred at room temperature for 20 hours. The reaction mixture was quenched with water (50 mL), extracted with ethyl acetate (50 mL, 25 mL). The combined organic layers were washed with 1N hydrochloric acid (3*10 mL), saturated aqueous sodium bicarbonate solution (2*10 mL), brine (10 mL), dried over anhydrous magnesium sulfate, filtered, and evaporated under reduced pressure. Diethyl ether was added to the residue, the resulting precipitate was collected by filtration, washed with diethyl ether, and dried under reduced pressure to afford the title compound (6.83 g, 16.5 mmol, 83%) as a white solid. 1H NMR (CDCl3) δ 1.23 (3H, t, J=7.1 Hz), 1.3-1.7 (4H, m), 1.44 (9H, s), 2.52 (3H, s), 2.5-2.8 (2H, m), 3.21 (2H, q, J=7.1 Hz), 3.65-3.9 (1H, m), 4.0-4.25 (2H, m), 7.28 (2H, d, J=8.4 Hz), 7.72 (2H, d, J=8.4 Hz).
  • 3
  • [ 53439-88-6 ]
  • [ 1129-25-5 ]
  • N-(1,3-dimethyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-5-yl)-4-(methylsulfanyl)benzene-1-sulfonamide [ No CAS ]
  • 4
  • [ 20870-91-1 ]
  • [ 1129-25-5 ]
  • N-(1-methyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-4-(methylsulfanyl)benzene-1-sulfonamide [ No CAS ]
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