Home Cart Sign in  
Chemical Structure| 54051-40-0 Chemical Structure| 54051-40-0

Structure of 54051-40-0

Chemical Structure| 54051-40-0

*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 [ 54051-40-0 ]

CAS No. :54051-40-0
Formula : C15H29NO
M.W : 239.40
SMILES Code : CC1(C)CCCC(C)(C)N1OC2CCCCC2

Safety of [ 54051-40-0 ]

Application In Synthesis of [ 54051-40-0 ]

* 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 [ 54051-40-0 ]

[ 54051-40-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2564-83-2 ]
  • [ 446065-11-8 ]
  • [ 54051-40-0 ]
YieldReaction ConditionsOperation in experiment
98% With silver(l) oxide; In water; toluene; at 20℃; for 0.166667h;Inert atmosphere; Sealed tube; Dried 10mL reaction tube was added <strong>[446065-11-8]cyclohexyl trifluoroborate potassium salt</strong> (19.0mg, 0.1mmol, 1.0 eq.),Silver oxide (25.4 mg, 0.1 mmol, 1.0 eq.) And 2,2,6,6-tetramethylpiperidine oxide (15.6 mg, 0.1 mmol,1. 0eq.), Exchanging the nitrogen three times, into a reaction tube under a nitrogen flow into 1. 0mL toluene and 20. 0muL distilled water, tighten the reaction tube cover, stirring vigorously at room temperature for 10 minutes, the reaction tube wall can be Clearly see the formation of silver mirror. The reaction mixture was first filtered through celite and the metal residue was filtered off. The filter cake was washed three times with ethyl acetate. The combined filtrates were spin-dried under reduced pressure to give 23.4 mg of a colorless oily liquid in 98% yield.
96% With silver(l) oxide; In water; toluene; at 25℃; for 0.166667h;Schlenk technique; Inert atmosphere; General procedure: In air, the potassium alkyltrifluoroborate (1.0 eq.), Ag2O (1.0 eq.) and TEMPO (1.0 eq.) were sequentially weighed and added to a screw-capped Schenk tube containing a magnetic stir bar. The vessel was evacuated and refilled with nitrogen for three times. Toluene (10.0 mL/mmol) and distilled water (200 muL/mmol) were added in turn under N2 atmosphere using syringes through a septum which was temporarily used to replace the screw cap. The reaction mixture was then vigorously stirred at room temperature for the indicated time. The resulting mixture was filtered through a pad of Celite, and the filter cake was washed with ethyl acetate (30 mL x 3). The combined filtrate was evaporated under vacuum to dryness and the residue was purified by column chromatography to yield the desired product.
  • 2
  • [ 2564-83-2 ]
  • [ 62-53-3 ]
  • [ 1571-08-0 ]
  • [ 446065-11-8 ]
  • [ 54051-40-0 ]
  • [ 24313-71-1 ]
 

Historical Records