Home Cart Sign in  
Chemical Structure| 1491142-16-5 Chemical Structure| 1491142-16-5

Structure of 1491142-16-5

Chemical Structure| 1491142-16-5

*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 [ 1491142-16-5 ]

CAS No. :1491142-16-5
Formula : C11H9N3O
M.W : 199.21
SMILES Code : O=C(C1=NC=CC(C2=CC=CC=C2)=N1)N

Safety of [ 1491142-16-5 ]

Application In Synthesis of [ 1491142-16-5 ]

* 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 [ 1491142-16-5 ]

[ 1491142-16-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1491142-16-5 ]
  • [ 74647-39-5 ]
YieldReaction ConditionsOperation in experiment
87% With sulfuric acid; at 100℃; General procedure: A mixture of an appropriate 4-substititedphenylpyrimidine-2-carboxamide (0.025mol) and 20% H2SO4 (100mL) was heated at 100C for 5-10h and monitored by TLC. The reaction mixture was poured onto ice/water with vigorously stirring and then the precipitatewas collected by filtration and dried to give the corresponding 4-substititedphenylpyrimidine-2-carboxylic acids as light yellow solids.
86% With sulfuric acid; at 100℃; for 10.0h; A mixture of intermediate c (5 g, 0.06 mol)Was added to 20% sulfuric acid (100 mL)100 C for 10 hours,After the completion of the reaction, the temperature was lowered to room temperature,Add 200 mL of water,Stirring for half an hour,Take filter cake, dry,To give a pale yellow solid, 4.3 g,Yield 86%.
47% With ethanol; sodium hydroxide; at 100℃; A solution of 2-cyano-4-phenylpyrimidine and 4-phenylpyrimidine-2-carboxamide (18?, 0.42 g, 2.4 mmol) in a 1 : 1 mixture of EtOH and NaOH solution (1 N) was allowed to stir at 100 C for 3 h. The resulting reaction mixture ws concentrated, water (20 mL) was added and the basic aqueous solution was acidified to pH 6 with concentrated HC1 to give 200 mg (47%) of 4-phenylpyrimidine-2-carboxylic acid (19?) as a yellow solid. NMR (CD3OD, 400 MHz) d 8.81 (br s, 1H), 8.38 (d, J= 6.7 Hz, 2H), 8 21 (br s, i l l). 7.68 - 7.22 (m, 3H). MS m/e: 201 ( I · 1 1 ) .
 

Historical Records