Home Cart Sign in  
Chemical Structure| 26524-91-4 Chemical Structure| 26524-91-4

Structure of 26524-91-4

Chemical Structure| 26524-91-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 26524-91-4 ]

CAS No. :26524-91-4
Formula : C9H8O2S
M.W : 180.22
SMILES Code : O=C(C1=CC=CC=C12)CCS2=O
MDL No. :MFCD14613832

Safety of [ 26524-91-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 26524-91-4 ]

* 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 [ 26524-91-4 ]

[ 26524-91-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3528-17-4 ]
  • [ 26524-91-4 ]
YieldReaction ConditionsOperation in experiment
73%Spectr. With diphenyl diselenide; urea hydrogen peroxide adduct; In dichloromethane; at 20℃; for 24h; General procedure: UHP (2 mmol) was dissolved in CH2Cl2 (2 mL), and the solutionwas stirred at r.t. A solution of Ph2Se2 (1 mol%) and sulfide (2mmol) in CH2Cl2 (2 mL) was added to the UHP solution. Themixture was stirred at r.t. for 24 h or until complete conversionto sulfoxide was observed by TLC. Extraction was carried outwith CH2Cl2 (3 × 5 mL), after the addition of H2O (5 mL), and thecombined organic solutions were washed with brine (50 mL),dried (MgSO4), filtered, and the solvents removed underreduced pressure. Sulfoxide products were purified where necessaryby column chromatography. Yellow oil; νmax (cm-1) 1694, 1585, 1325, 1282, 1237, 1182, 1120, 1080, 1039, 854; 1H NMR (400MHz, CDCl3): δH 2.86-2.97 (1 H, m), 3.43-3.56 (3 H, m), 7.65-7.68 (1 H, m), 7.75-7.79 (1 H, m),7.87 (1 H, dd, J 8.1, 7.6 Hz), 8.14 (1 H, dd, J 8.0, 7.6 Hz) ppm; 13C NMR (100 MHz, CDCl3): δC30.3, 46.6, 128.5, 128.9, 132.1, 134.6, 145.5, 192.1
 

Historical Records