Home Cart Sign in  
Chemical Structure| 307302-08-5 Chemical Structure| 307302-08-5

Structure of 307302-08-5

Chemical Structure| 307302-08-5

*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 [ 307302-08-5 ]

CAS No. :307302-08-5
Formula : C15H14O3
M.W : 242.27
SMILES Code : O=C(O)C1=CC=CC(OCC2=CC=C(C)C=C2)=C1
MDL No. :MFCD09712906

Safety of [ 307302-08-5 ]

Application In Synthesis of [ 307302-08-5 ]

* 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 [ 307302-08-5 ]

[ 307302-08-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 307302-08-5 ]
  • [ 79-37-8 ]
  • [ 29608-05-7 ]
  • [ 307302-10-9 ]
YieldReaction ConditionsOperation in experiment
With sodium chloride; triethylamine; In tetrahydrofuran; water; N,N-dimethyl-formamide; Example 85 (Production of Compound 85) To 3-(4-methylbenzyloxy)benzoic acid (1.00 g) dissolved in THE (15 ml) were added oxalyl chloride (468 oil) and one drop of DMF, and the resulting mixture was stirred at room temperature for one hour. After the reaction mixture was evaporated under reduced pressure to remove the solvent, to the residue dissolved in THF (15 ml) were added at room temperature <strong>[29608-05-7]1-(4-aminobenzyl)piperidine</strong> (864 mg) and triethylamine (695 mul). The resulting mixture was stirred at room temperature for 3 hours, was then mixed with water (100 ml) and was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride, was dried with anhydrous sodium sulfate and was then evaporated under reduced pressure to remove the solvent. The resulting residue was recrystallized from ethyl acetate/hexane to obtain 3-(4-methylbenzyloxy)-4'-(piperidinomethyl)benzanilide (compound 85) (1.25 g) as colorless crystals.
  • 2
  • [ 307302-08-5 ]
  • [ 29608-05-7 ]
  • [ 307302-10-9 ]
 

Historical Records

Technical Information

Categories