Home Cart Sign in  
Chemical Structure| 1425932-71-3 Chemical Structure| 1425932-71-3

Structure of 1425932-71-3

Chemical Structure| 1425932-71-3

*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 [ 1425932-71-3 ]

CAS No. :1425932-71-3
Formula : C13H12BrF3N2O
M.W : 349.15
SMILES Code : FC(C1=CC2=C(C(Br)=C1)C=NN2C3CCCCO3)(F)F

Safety of [ 1425932-71-3 ]

Application In Synthesis of [ 1425932-71-3 ]

* 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 [ 1425932-71-3 ]

[ 1425932-71-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-87-2 ]
  • [ 1000342-95-9 ]
  • [ 1425932-71-3 ]
YieldReaction ConditionsOperation in experiment
78% With toluene-4-sulfonic acid; In tetrahydrofuran; for 18h;Inert atmosphere; Reflux; Referential example 25 (l-(Tetrahydro-2H-pyran-2-yl)-6-(trifluoromethyl)-lH-indazol-4-yl)methanamine (127) step 1 : A round-bottom flask was charged with 4-bromo-6-(trifluoromethyl)-lH-indazole (1.00 g, 3.8 mmol), TsOH monohydrate (27 mg, 0.15 mmol), 3,4-dihydro-2H-pyran (1.59 g, 18.9 mmol), and THF (25 mL). The reaction mixture was degassed with nitrogen and heated under reflux for 18 h, and then the solvent was removed in vacuo. The residue was purified by S1O2 chromatography to afford 4-bromo-l - (tetrahydro-2H-pyran-2-yl)-6-(trifluoromethyl)-lH-indazole (1.03 g, 78percent) as a yellow oil. MS (ESI) m/z: 265.2 [(M - THP group)+l]+.
 

Historical Records