Home Cart Sign in  
Chemical Structure| 909871-48-3 Chemical Structure| 909871-48-3

Structure of 909871-48-3

Chemical Structure| 909871-48-3

*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 [ 909871-48-3 ]

CAS No. :909871-48-3
Formula : C24H24O4
M.W : 376.45
SMILES Code : O=C(O)C1=CC(C(C)C)=C(OCC2=CC=CC=C2)C=C1OCC3=CC=CC=C3
MDL No. :MFCD28965489

Safety of [ 909871-48-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 909871-48-3 ]

* 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 [ 909871-48-3 ]

[ 909871-48-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 909871-48-3 ]
  • [ 63572-73-6 ]
  • 2,4-dihydroxy-5-isopropyl-N-(1H-pyrazolo[3,4-b]pyridin-5-yl)benzamide [ No CAS ]
  • 2
  • [ 909871-48-3 ]
  • [ 63572-73-6 ]
  • 2,4-bis(benzyloxy)-5-isopropyl-N-(1H-pyrazolo[3,4-b]pyridin-5-yl)benzamide [ No CAS ]
  • 3
  • [ 580-15-4 ]
  • [ 909871-48-3 ]
  • 2,4-bis(benzyloxy)-5-isopropyl-N-(quinolin-6-yl)benzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
53% With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20℃; for 12h;Inert atmosphere; General procedure: 2,4-Bis(benzyloxy)-5-isopropylbenzoic acid (1.28 g, 3.4 mmol), N-methylmorpholine (0.9 mL), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide)(0.97 g, 5.1 mmol) and hydroxybenzotriazole (0.55 g,4.1 mmol) were added to a solution of 3-aminoquinoline (23) (0.5 g,3.4 mmol) in DMF (5 mL). The reaction mixture was stirred at rt for 12 h and then diluted with water. Extraction was with EtOAc (3×50 mL), and the organic layer was dried over anhydrous MgSO4, filtered, and concentrated. The residue was purified by silica gel chromatography(EtOAc:n-hexane=1:3) to afford compound 6 (1.03 g,61% yield).
 

Historical Records