Home Cart Sign in  
Chemical Structure| 219551-85-6 Chemical Structure| 219551-85-6

Structure of 219551-85-6

Chemical Structure| 219551-85-6

*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 [ 219551-85-6 ]

CAS No. :219551-85-6
Formula : C17H14O4
M.W : 282.29
SMILES Code : O=C1C(CC2=CC=CC=C2)=C(C)C3=C(O1)C=C(O)C=C3O

Safety of [ 219551-85-6 ]

Application In Synthesis of [ 219551-85-6 ]

* 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 [ 219551-85-6 ]

[ 219551-85-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6099-90-7 ]
  • [ 620-79-1 ]
  • [ 219551-85-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In ethanol; a) 3-Benzyl-5,7-dihydroxy-4-methyl-2H-1-benzopyran-2-one A solution of <strong>[6099-90-7]phloroglucinol dihydrate</strong> (20 g) and ethyl 2-benzylacetoacetate (27.5 ml) in ethanol (320 ml) was treated with dry HCl at 0 C. for five hours and the solution was kept at that temperature overnight. The yellow solution was concentrated and triturated with water, the solids filtered, washed with water and dried. The resulting hydrate was thrice evaporated to dryness from toluene, triturated with petroleum ether (bp. 40-60 C.) and filtered. Yield 33,4 g (96%). Melting point 258-260 C. 1H-NMR (DMSO-d6, 400 MHz): 2.525 (s, 3H, CH3), 3.887 (s, 2 H, CH2Ph), 6.171 (d, 1H, J=2,4 Hz), 6.274 (d, 1H, J=2,4 Hz), 7.167-7.279 (m, 5H, Ph), 10.2 (s,1H, OH), 10.47 (s, 1H, OH).
With hydrogenchloride; In ethanol; a 3-Benzyl-5,7-dihydroxy-4-methyl-2H -1 -benzopyran-2-one STR8 A solution of <strong>[6099-90-7]phloroglucinol dihydrate</strong> (20 g) and ethyl 2-benzylacetoacetate (27.5 ml) in ethanol (320 ml) was treated with dry HCl at 0 C. for five hours and the solution was kept at that temperature overnight. The yellow solution was concentrated and triturated with water, the solids filtered, washed with water and dried. The resulting hydrate was thrice evaporated to dryness from toluene, triturated with pethroleum ether (bp. 40-60 C.) and filtered. Yield 33,4 g (96%). Melting point 258-260 C. 1 H-NMR (DMSO-d6, 400 MHz): 2.525 (s, 3H, CH3), 3.887 (s, 2 H, CH2 Ph), 6.171 (d,1H, J=2,4 Hz), 6.274 (d,1H, J=2,4 Hz), 7.167-7.279 (m, 5H, Ph), 10.2 (s, 1H, OH), 10.47 (s, 1H, OH).
  • 2
  • [ 71-33-0 ]
  • [ 219551-85-6 ]
  • 6-(3-benzyl-5,7-dihydroxy-4-methyl-2-oxo-2H-chromen-8-yl)-1,3,5-triazinane-2,4-dione [ No CAS ]
YieldReaction ConditionsOperation in experiment
64% With trifluoroacetic acid; In chloroform; for 4h;Reflux; General procedure: 5,7-Dihydroxycoumarin 5a-e (1 mmol) and triazine 10 (1mmol) were dissolved in TFA (10 mL) and CHCl3 (10 mL), and the reaction solution was heated under reflux for 4 h. Then to the reaction mixture was added 2-PrOH (15 mL), the mixture was cooled, and the precipitate was filtered off. The product 11a-e was recrystallized from 1,4-dioxane and dried at 100C for 4 h
 

Historical Records