Home Cart Sign in  
Chemical Structure| 2168-78-7 Chemical Structure| 2168-78-7

Structure of 2168-78-7

Chemical Structure| 2168-78-7

*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 [ 2168-78-7 ]

CAS No. :2168-78-7
Formula : C8H8S2
M.W : 168.28
SMILES Code : S=C(SC)C1=CC=CC=C1
MDL No. :MFCD00799285

Safety of [ 2168-78-7 ]

Application In Synthesis of [ 2168-78-7 ]

* 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 [ 2168-78-7 ]

[ 2168-78-7 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 2168-78-7 ]
  • [ 22259-53-6 ]
  • [ 866836-59-1 ]
  • 2
  • [ 21109-25-1 ]
  • [ 2168-78-7 ]
  • [ 943188-12-3 ]
  • 3
  • [ 5760-20-3 ]
  • [ 2168-78-7 ]
  • [ 1576-35-8 ]
  • 1-phenyl-3-(p-tolylthio)imidazo[1,5-a]quinoline [ No CAS ]
  • 4
  • [ 5760-20-3 ]
  • [ 2168-78-7 ]
  • [ 1950-68-1 ]
  • 3-((4-methoxyphenyl)thio)-1-phenylimidazo[1,5-a]quinoline [ No CAS ]
  • 5
  • [ 5760-20-3 ]
  • [ 2168-78-7 ]
  • 4-(trifluoromethyl)benzenesulfonyl hydrazide [ No CAS ]
  • C24H15F3N2S [ No CAS ]
  • 6
  • [ 5760-20-3 ]
  • [ 2168-78-7 ]
  • 1-phenylimidazo<1,5-a>quinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
81% General procedure: To a solution of dithioester (1.0 eq, 1.0 mmol) inTHF (2 mL) was added amine or hydrazine (1.1 eq, 1.1 mmol) at room temperature, the resulting mixture was stirred for 45 min. monitored the dithioester could no longer be detected. To the above mixture was added I2 (2.0 equiv. The mixture was stirred at room temperature for 1.5 h and progress was monitored by TLC. The reaction mixture was diluted with EtOAc neutralized with saturated sodium bicarbonate solution, separated organic layer; the aqueous layer was extracted with EtOAc (25 mL X 3). The combined organic layers were washed with water, dried over anhydrous Na2SO4. The solvent was removed under reduced pressure; the residue was purified by silicagel chromatography.
 

Historical Records