Home Cart Sign in  
Chemical Structure| 1146-44-7 Chemical Structure| 1146-44-7

Structure of 1146-44-7

Chemical Structure| 1146-44-7

*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 [ 1146-44-7 ]

CAS No. :1146-44-7
Formula : C12H8Cl2O2S2
M.W : 319.23
SMILES Code : O=S(C1=CC=C(Cl)C=C1)(SC2=CC=C(Cl)C=C2)=O

Safety of [ 1146-44-7 ]

Application In Synthesis of [ 1146-44-7 ]

* 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 [ 1146-44-7 ]

[ 1146-44-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1146-44-7 ]
  • [ 538-28-3 ]
  • [ 933-01-7 ]
  • [ 1142-19-4 ]
  • [ 29391-11-5 ]
  • 2
  • [ 14752-66-0 ]
  • [ 106-54-7 ]
  • [ 1146-44-7 ]
YieldReaction ConditionsOperation in experiment
94% With iron(III) chloride; In N,N-dimethyl-formamide; at 20℃; for 0.833333h;Green chemistry; General procedure: A mixture of the appropriate thiol 1 (0.5 mmol), sodium thiosulfinate 2 (1.0 mmol), and FeCl3 (20 mol%) in DMF (3 mL) was stirred at r.t. for 30-60 min under air in a round-bottomed flask.When the reaction was complete (TLC), H2O (5 mL) was added and the mixture was extracted with EtOAc (3 × 5 mL). The combined organic phases were dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by column chromatography using a gradient mixture of hexane and EtOAc as eluent
66% With sodium iodide; In acetonitrile; at 20℃; for 4h;Electrochemical reaction; Green chemistry; General procedure: In an oven-dried undivided three-necked bottle (25 mL) equipped with a stir bar, benzenesulfinate salt 1a (0.6 mmol), thiols 2a (0.3 mmol), sodium iodide (0.2 equiv), MeCN (5 mL) was added. The bottle was equipped with platinum plate (10 mm×10 mm) as the anode and platinum plate (10 mm×10 mm) as the cathode. The reaction mixture was stirred and electrolyzed at a constant current of 10 mA at room temperature for 4 h. After completion of the reaction, as indicated by TLC and GC-MS, the pure product was obtained by flash column chromatography on silica gel (petroleum ether : ethyl acetate = 40-30 : 1). The same procedure was applied to the production of other compounds 3a-p.
 

Historical Records

Technical Information

Categories