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[ CAS No. 88040-86-2 ] {[proInfo.proName]}

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Chemical Structure| 88040-86-2
Chemical Structure| 88040-86-2
Structure of 88040-86-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 88040-86-2 ]

CAS No. :88040-86-2 MDL No. :MFCD00060552
Formula : C8H9ClO3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 220.67 Pubchem ID :-
Synonyms :

Safety of [ 88040-86-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501 UN#:1759
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 88040-86-2 ]

* 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 [ 88040-86-2 ]

[ 88040-86-2 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 252978-89-5 ]
  • [ 88040-86-2 ]
  • 5-methyl-2-methoxyl-[4-(1-piperazinyl)-1H-indol-1-yl]sulfonyl}phenyl ether hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 18 5-Methyl-2-methoxyl-[4-(1-piperazinyl)-1H-indol-1-yl]sulfonyl}phenyl Ether Hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 5-methyl-2-methoxyphenylsulfonyl chloride according to Method 3: 1H NMR (270 MHz, DMSO-d6) delta 9.45 (br, 1H), 7.92 (d, J=8 Hz, 1H), 7.70 (d, J=5 Hz, 1H), 7.30 (d, J=8 Hz, 1H), 7.13 (t,J=8Hz, 1H), 7.01-6.92 (m, 2H), 6.83 (d,J=5Hz, 1H), 6.73 (d,J=8Hz, 1H), 3.70 (s, 3H), 3.26 (m, 8H), 3.32 (s, 3H); MS (ESI+) for m/z 386 (M+H)+.
  • 3
  • [ 504-15-4 ]
  • [ 88040-86-2 ]
  • [ 197959-95-8 ]
YieldReaction ConditionsOperation in experiment
54% With sodium hydrogencarbonate In diethyl ether; water at 20℃; for 72h; 14.a a) a) 3-(2-Methoxy-5-methylphenylsulfonyloxy)-5-methylphenol To a solution of 1.00 g (8.05 mmol) of orcinol monohydrate and 1.63 g (7.38 mmol) of 2-methoxy-m-toluenesulfonyl chloride in 20 mL of diethyl ether was added 20 mL of saturated aqueous NaHCO3 and the biphasic mixture stirred vigorously at ambient temperature for 3 days. The layers were separated and the aqueous layer extracted with 2 x 30 mL of ethyl acetate. The combined organic layers were washed with 50 mL of brine, dried (Na2SO4) and concentrated to give 2.2 g of an orange syrup. Crystallization from dichloromethane-hexane (two crops) afforded 1.24 g (54%) of the title compound as a light orange powder: 1H-NMR (300 MHz; CDCl3) δ 7.62 (d, 1 H, J = 2.0 Hz), 7.40 (m, 1 H), 6.96 (d, 1 H, J = 8.5 Hz), 6.52 (m, 2 H), 6.42 (t, 1 H, J = 2.1 Hz), 5.13 (s, 1 H), 3.96 (s, 3 H), 2.29 (s, 3 H) and 2.23 (s, 3 H).
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