Home Cart Sign in  
Chemical Structure| 6973-84-8 Chemical Structure| 6973-84-8

Structure of 6973-84-8

Chemical Structure| 6973-84-8

*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 [ 6973-84-8 ]

CAS No. :6973-84-8
Formula : C9H8OS2
M.W : 196.29
SMILES Code : OC(C1=CC=CS1)C2=CC=CS2
MDL No. :MFCD03211768

Safety of [ 6973-84-8 ]

Application In Synthesis of [ 6973-84-8 ]

* 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 [ 6973-84-8 ]

[ 6973-84-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 704-38-1 ]
  • [ 6973-84-8 ]
YieldReaction ConditionsOperation in experiment
79% With sodium tetrahydroborate; In tetrahydrofuran; water; for 2h;Reflux; General procedure: To a solution of the corresponding ketone 1 (1mmol) in THF (2 mL), water (0.06 mL) and NaBH4 (1.25mmol, 0.047 g) were added. The mixture was heated at reflux for 2 h. Then, the solution was diluted with water (10 mL) and THF was evaporated. The residue was extracted with ethyl acetate. The combined organic layers were dried over MgSO4. The solvent was evaporated and crude products were purified by CC (SiO2, petroleum ether/ethyl acetate 8:2).
54% With diisobutylaluminium hydride; In methanol; hexane; dichloromethane; ethyl acetate; Example 9 Methyl [[bis-(2-thienyl)methyl]thio]acetate To a -35 to -40 C. solution of <strong>[704-38-1]2-(then-2-oyl)thiophene</strong> (Maybridge of Cornwall, UK) (500 mg, 2.60 mmol) in 10 mL of methylene chloride, is added dropwise a 1M solution of diisobutylaluminum hydride in methylene chloride (6.50 mL, 6.50 mmol) over 20 minutes. The reaction is stirred at -40 C. for 2.5 hours and then quenched by the slow addition of 10 mL of methanol. The mixture is warmed to room temperature and poured into 100 mL of saturated aqueous sodium tartrate. The aqueous solution is extracted with several portions of methylene chloride, the organic extracts combined, and dried over magnesium sulfate. Chromatography on silica gel, eluding with a 1:2 mixture of ethyl acetate to hexane, gives di-2-thienylmethanol as a light orange solid in 54% yield.
  • 3
  • [ 704-38-1 ]
  • C16H10N2S2 [ No CAS ]
  • [ 6973-84-8 ]
 

Historical Records

Technical Information

Categories