Home Cart Sign in  
Chemical Structure| 73013-67-9 Chemical Structure| 73013-67-9

Structure of 73013-67-9

Chemical Structure| 73013-67-9

*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 [ 73013-67-9 ]

CAS No. :73013-67-9
Formula : C16H10N2
M.W : 230.26
SMILES Code : N#CC1=CC2=CC=CC=C2N=C1C3=CC=CC=C3
MDL No. :MFCD22573688

Safety of [ 73013-67-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 73013-67-9 ]

* 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 [ 73013-67-9 ]

[ 73013-67-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1006-67-3 ]
  • [ 529-23-7 ]
  • [ 73013-67-9 ]
YieldReaction ConditionsOperation in experiment
33% With [RuCl2pentamethylcyclopentadiene]n; silver trifluoroacetate; trifluoroacetic acid; In 2,2,2-trifluoroethanol; at 80℃; for 8h; The preparation method of compound I-25,Including the following process: 0.2mmol of 2-aminobenzaldehyde,<strong>[1006-67-3]5-phenylisoxazole</strong> 0.3mmol,Dichloro (pentamethylcyclopentadienyl) ruthenium () 0.005mmol,Silver trifluoroacetate 0.02mmol,Add 0.2mmol trifluoroacetic acid to the reaction tube,Dissolved in an appropriate amount of trifluoroethanol solvent,React at 80 for 8 hours,The reaction solution was filtered through diatomaceous earth, and the filtrate was concentrated,Purification by column chromatography gave 15.0 mg of the target product with a yield of 33%.
33% With bis[dichloro(pentamethylcyclopentadienyl)ruthenium(III)]; silver trifluoroacetate; trifluoroacetic acid; In 2,2,2-trifluoroethanol; at 80℃; for 10h; General procedure: A reaction tube (15 mL) equipped with a magnetic stirrer bar was charged with 2-aminobenzaldehyde 1a (0.1 mmol), isoxazole 2a (0.12 mmol), [Cp*RuCl2]2 (2.5 mol %), CF3COOAg (10 mol %), CF3COOH (1 equiv.) in anhydrous CF3CH2OH (1.5 mL). The reaction mixture was stirred at 80 for 10 h under air atmosphere. When the reaction was completed, the mixture was cooled to room temperature and then purified by column chromatography on silica gel with ethyl acetate/petroleum ether (1:5) to give the desired product 3a.
 

Historical Records

Technical Information

Categories