Home Cart Sign in  
Chemical Structure| 160037-60-5 Chemical Structure| 160037-60-5

Structure of 160037-60-5

Chemical Structure| 160037-60-5

*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 [ 160037-60-5 ]

CAS No. :160037-60-5
Formula : C13H16N2O3
M.W : 248.28
SMILES Code : O=C(OCC)/C(C(C1=CC=NC=C1)=O)=C/N(C)C

Safety of [ 160037-60-5 ]

Application In Synthesis of [ 160037-60-5 ]

* 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 [ 160037-60-5 ]

[ 160037-60-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 160037-60-5 ]
  • [ 658-27-5 ]
  • 1-(3-fluorophenyl)-5-pyridin-4-yl-1H-pyrazole-4-carboxylic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
In acetic acid;Heating / reflux; 4b) l-(3-FluorophenylV5-pyridin-4-yl-lH-pyrazole-4-carboxylic acid ethyl ester; To 3-Dimethylamino-2-(pyridine-4-carbonyl)-acrylic acid ethyl ester (3.34 g, 13.5 mmol) in glacial acetic acid (30 ml) is added l-(3-fluorophenyl) hydrazine (13.5 mmol) and the mixture is refluxed overnight. The reaction mixture is poured into water (50 ml) and extracted with chloroform (3x15 ml). The combined organic phases are washed with 5% sodium hydrogencarbonate (2 x 20 ml), water (2 x 20 ml) and then dried with magnesium sulphate. The solvent is evaporated and the residue is purified by chromatography using hexane / ethyl acetate (1:1) as eluent to give the titled compound.
 

Historical Records