Home Cart Sign in  
Chemical Structure| 412947-46-7 Chemical Structure| 412947-46-7

Structure of 412947-46-7

Chemical Structure| 412947-46-7

*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 [ 412947-46-7 ]

CAS No. :412947-46-7
Formula : C8H6ClN
M.W : 151.59
SMILES Code : NC1=CC=C(Cl)C=C1C#C

Safety of [ 412947-46-7 ]

Application In Synthesis of [ 412947-46-7 ]

* 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 [ 412947-46-7 ]

[ 412947-46-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19591-17-4 ]
  • [ 412947-46-7 ]
  • [ 1301267-84-4 ]
YieldReaction ConditionsOperation in experiment
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In tetrahydrofuran; at 20℃;Inert atmosphere; General procedure: Under the protection of nitrogen, a THF solution (20 mL) containing Et3N (15 mmol) and o-ethynylaniline (6 mmol) was added to a flask containing amide (5 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.1 mmol) and CuI (0.05 mmol). The mixture was stirred overnight at room temperature (monitored by TLC). Then the solvent was removed under vacuum. The obtained residue was treated with a mixture of chloroform (30 mL) and water (30 mL). The separated organic layer was washed with brine (15 mL), dried with anhydrous MgSO4. After filtration, the filtrate was concentrated and the residue was purified by chromatography on silica gel (EtOAc-PE, 1:2) to give N-[2-[(2-Aminophenyl)ethynyl]phenyl]amide.
 

Historical Records