Home Cart Sign in  
Chemical Structure| 21487-48-9 Chemical Structure| 21487-48-9

Structure of 21487-48-9

Chemical Structure| 21487-48-9

*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 [ 21487-48-9 ]

CAS No. :21487-48-9
Formula : C11H10N2O
M.W : 186.21
SMILES Code : O=CC1=CN(C2=CC=CC=C2)N=C1C
MDL No. :MFCD02705915

Safety of [ 21487-48-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H319
Precautionary Statements:P264-P280-P305+P351+P338-P337+P313

Application In Synthesis of [ 21487-48-9 ]

* 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 [ 21487-48-9 ]

[ 21487-48-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3199-50-6 ]
  • [ 21487-48-9 ]
  • [ 1570069-59-8 ]
YieldReaction ConditionsOperation in experiment
93% With sodium hydroxide; In ethanol; at 0 - 20℃; General procedure: Aqueous sodium hydroxide (12 mmol) was added to a mixture of appropriate ketone (10 mmol) and 1, 3-disubstituted-1H-pyrazole-4-carbaldehyde (10 mmol) in ethanol at 0 C. The resulting reaction mixture was allowed to stir for 6-8 h at room temperature. The reaction was monitored by TLC and upon completion, the reaction mixture was poured into iced water. The pH of the mixture was adjusted to 6 using a 0.01 N HCl solution. The precipitates were filtered and recrystallized from ethanol to obtain the compounds 3a-m in 40-93% yield.
93% With water; sodium hydroxide; In ethanol; at 0 - 20℃; General procedure: To a mixture of 2-acetylthiophene (1 mL, 0.0092 mol) and 3-methyl-1-phenyl-1H-pyrazole-4-yl (1.72 g, 0.0092 mol) in ethanol was added aqueous sodium hydroxide (0.44 g, 0.011 mol) at 0 oC. The resulting reaction mixture was allowed to stir for 6-8 h at room temperature. The reaction was monitored by TLC and on completion, reaction mixture was poured into ice coldwater. Then pH of the mixture adjusted to 6 using 0.01 N HCl solution. The obtained precipitates were filtered, dried and recrystallized from ethanol to get the compound 3a. Remaining compounds (3b-j) were prepared according to this procedure.
  • 2
  • [ 3199-50-6 ]
  • [ 21487-48-9 ]
  • (E)-1-(5-bromofuran-2-yl)-3-(3-methyl-1-phenyl-1H-pyrazole-4-yl)prop-2-en-1-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With sodium hydroxide; In ethanol; water; at 0 - 20℃; The starting material 1,3-disubstituted-1H-pyrazole-4-carbaldehydes were prepared according to the literatureprocedure[29]. To a mixture of an appropriateacetophenone (1, 10 mmol) and 1,3-disubstituted-1H-pyrazole-4-carbaldehyde (2,10 mmol) in ethanol wasadded aqueous sodium hydroxide (12 mmol ) at 0 C. Theresulting reaction mixture was allowed to stir for 6-8 h atroom temperature. The reaction was monitored by TLCand on its completion, the reaction mixture was pouredinto ice-cold water. Then pH of the mixture adjusted to 6using 0.01N HCl solution. Thus, obtained product wasfiltered and recrystallized from ethanol to give the pure 3a. Rest compounds were synthesized according to thisprocedure to obtain compounds 3b-k in good to excellentyield.
 

Historical Records

Technical Information

Categories