[ CAS No. 5908-62-3 ]

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Cat. No.: {[proInfo.prAm]}
2D
Chemical Structure| 5908-62-3
Chemical Structure| 5908-62-3
Structure of 5908-62-3

Quality Control of [ 5908-62-3 ]

Purity: {[proInfo.showProBatch.pb_purity]}

Related Doc. of [ 5908-62-3 ]

SDS

Product Details of [ 5908-62-3 ]

CAS No. :5908-62-3MDL No. :MFCD09802220
Formula :C3H7NO2SBoiling Point :224.1°C at 760 mmHg
Linear Structure Formula :C3H7SO2NInChI Key :-
M.W :121.16Pubchem ID :-
Synonyms :

Computed Properties of [ 5908-62-3 ]

TPSA : - H-Bond Acceptor Count : -
XLogP3 : - H-Bond Donor Count : -
SP3 : - Rotatable Bond Count : -

Safety of [ 5908-62-3 ]

Signal Word:WarningClassN/A
Precautionary Statements:P280-P305+P351+P338UN#:N/A
Hazard Statements:H302Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 5908-62-3 ]

  • Upstream synthesis route of [ 5908-62-3 ]
  • Downstream synthetic route of [ 5908-62-3 ]

[ 5908-62-3 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 35578-28-0 ]
  • [ 5908-62-3 ]
YieldReaction ConditionsOperation in experiment
100% With sodium ethanolate In ethanol at 20℃; for 5.00 h; Heating / reflux To a solution of 3-CHLORO-1-PROPANESULFONAMIDE (D21A) (27 g, 170 mmol, 1 equiv) in EtOH (250 mi) at room temperature was added NaOEt (11.7 g, 170 MMOL, 1 equiv). The resulting mixture was refluxed for 5 h then cooled to room temperature and concentrated in vacuo. The residual solid was extracted thoroughly with CH2CI2 and the extracts were concentrated in vacuo to give isothiazolidine 1,1-dioxide (D22a) (20 g, 100percent).
Reference: [1] Patent: WO2004/50619, 2004, A1. Location in patent: Page 24
[2] Journal of the American Chemical Society, 2015, vol. 137, # 17, p. 5638 - 5641
[3] Journal of Organic Chemistry, 1987, vol. 52, # 11, p. 2162 - 2166
[4] Patent: WO2012/3283, 2012, A1. Location in patent: Page/Page column 206-207
[5] Patent: US2012/316147, 2012, A1. Location in patent: Page/Page column 62-63
[6] Patent: WO2012/168350, 2012, A1. Location in patent: Page/Page column 133; 134
[7] DRP/DRBP Org.Chem.,
  • 2
  • [ 21896-59-3 ]
  • [ 5908-62-3 ]
Reference: [1] Organic Letters, 2003, vol. 5, # 22, p. 4175 - 4177
  • 3
  • [ 63132-74-1 ]
  • [ 5908-62-3 ]
Reference: [1] Organic Letters, 2003, vol. 5, # 22, p. 4175 - 4177
  • 4
  • [ 556-53-6 ]
  • [ 5908-62-3 ]
Reference: [1] Chemische Berichte, 1963, vol. 96, p. 3068 - 3075
[2] Patent: DE932676, 1953,
[3] Patent: GB752227, 1954,
[4] Patent: US2866786, 1954,
[5] Patent: GB786059, 1954,
[6] Chemische Berichte, 1963, vol. 96, p. 3068 - 3075
[7] Patent: DE932676, 1953,
[8] Patent: GB752227, 1954,
[9] Patent: US2866786, 1954,
[10] Patent: GB786059, 1954,
  • 5
  • [ 463-22-9 ]
  • [ 5908-62-3 ]
  • [ 93531-48-7 ]
Reference: [1] Journal of Organic Chemistry, 1990, vol. 55, # 9, p. 2580 - 2586
[2] Journal of Organic Chemistry, 1990, vol. 55, # 9, p. 2580 - 2586
[3] Journal of Organic Chemistry, 1990, vol. 55, # 9, p. 2580 - 2586
  • 6
  • [ 107-10-8 ]
  • [ 5908-62-3 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 3, p. 757 - 760
  • 7
  • [ 108214-47-7 ]
  • [ 1120-71-4 ]
  • [ 5908-62-3 ]
  • [ 15909-83-8 ]
Reference: [1] Journal of Organic Chemistry, 1987, vol. 52, # 11, p. 2162 - 2166
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