Home Cart Sign in  
Chemical Structure| 86549-28-2 Chemical Structure| 86549-28-2

Structure of 86549-28-2

Chemical Structure| 86549-28-2

*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 [ 86549-28-2 ]

CAS No. :86549-28-2
Formula : C14H15NSi
M.W : 225.36
SMILES Code : C[Si](C)(C)C#CC1=CN=CC2=C1C=CC=C2
MDL No. :MFCD23135823

Safety of [ 86549-28-2 ]

Application In Synthesis of [ 86549-28-2 ]

* 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 [ 86549-28-2 ]

[ 86549-28-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 55270-33-2 ]
  • [ 1066-54-2 ]
  • [ 86549-28-2 ]
YieldReaction ConditionsOperation in experiment
78% 10.0 g (39.21 mmol) of <strong>[55270-33-2]4-iodo-isoquinoline</strong>, 280 mg (0.39 mmol) of PdCl2(PPh3)2, and 75 mg (0.39 mmol) of CuI were added to 180 mL of a mixture of anhydrous toluene and diisopropylamine (in a volume ratio of 5:1), and the mixture was stirred at room temperature for 5 minutes. Then, 8.4 mL (58.81 mmol) of ethynyltrimethylsilane was gradually added thereto, and the mixture was stirred at 80 C. for 18 hours. After the reaction was terminated, 50 mL of distilled water was added thereto, and the resultant was subjected to extraction three times with 50 mL of methylene chloride to obtain an organic layer. The organic layer was collected and dried with magnesium sulfate to evaporate the solvent. The residue was separately purified using silica gel column chromatography to obtain 6.9 g (30.62 mmol) of Intermediate 12(1) (Yield: 78%). The produced compound was identified using LC-MS. [0148] C14H15NSi: M+226.10
78% A. Synthesis of Intermediate 12(1)[0134] 10.0 g (39.21 mmol) of <strong>[55270-33-2]4-iodo-isoquinoline</strong>, 280 mg (0.39 mmol) of PdCl2(PPh3)2, and 75 mg (0.39 mmol) ofCul were added to 180 mL of a mixture of anhydrous toluene and diisopropylamine (in a volume ratio of 5:1), and themixture was stirred at room temperature for 5 minutes. Then, 8.4 mL (58.81 mmol) of ethynyltrimethylsilane was graduallyadded thereto, and the mixture was stirred at 80C for 18 hours. After the reaction was terminated, 50 mL of distilledwater was added thereto, and the resultant was subjected to extraction three times with 50 mL of methylene chloride toobtain an organic layer. The organic layer was collected and dried with magnesium sulfate to evaporate the solvent.The residue was separately purified using silica gel column chromatography to obtain 6.9 g (30.62 mmol) of Intermediate12(1) (Yield: 78 %). The produced compound was identified using LC-MS.C14H15NSi : M+ 226.10
 

Historical Records