Home Cart Sign in  
Chemical Structure| 1426654-03-6 Chemical Structure| 1426654-03-6

Structure of 1426654-03-6

Chemical Structure| 1426654-03-6

*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 [ 1426654-03-6 ]

CAS No. :1426654-03-6
Formula : C17H14FN3O3
M.W : 327.31
SMILES Code : O=C(OC)C1=CC=C(F)C(NC(C2=CN=C3C=C(C)C=CN32)=O)=C1
MDL No. :MFCD29918635

Safety of [ 1426654-03-6 ]

Application In Synthesis of [ 1426654-03-6 ]

* 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 [ 1426654-03-6 ]

[ 1426654-03-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 21801-80-9 ]
  • [ 369-26-6 ]
  • [ 1426654-03-6 ]
YieldReaction ConditionsOperation in experiment
To a suspension of 7-methylimidazo[1 ,2-a]pyridine-3-carboxylic acid (13f) (1 g, 5.68 mmol) in dichloromethane (300 mL) oxalyl chloride (2.4 mL, 28.4 mmol) and catalytic amounts of DMF. The resulting solution was stirred overnight at room temperature and concentrated under vacuum. The solid obtained was added into a solution of methyl 3- amino-4-fluorobenzoate (7) (1 .05 g, 6.24 mmol) in dry pyridine. The resulting solution was stirred (50°C) for 5 hours before it was poured into water. The solids were collected by filtration and used without further purification to yield methyl 4-fluoro-3-(7- methylimidazo[1 ,2-a]pyridine-3-carboxamido)benzoate (31 ).
 

Historical Records