Home Cart Sign in  
Chemical Structure| 15777-59-0 Chemical Structure| 15777-59-0

Structure of 15777-59-0

Chemical Structure| 15777-59-0

*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 [ 15777-59-0 ]

CAS No. :15777-59-0
Formula : C8H6BrN3
M.W : 224.06
SMILES Code : BrC1=NNC(C2=CC=CC=C2)=N1
MDL No. :MFCD13188619

Safety of [ 15777-59-0 ]

Application In Synthesis of [ 15777-59-0 ]

* 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 [ 15777-59-0 ]

[ 15777-59-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4922-98-9 ]
  • [ 15777-59-0 ]
YieldReaction ConditionsOperation in experiment
11 g With hydrogen bromide; sodium nitrite; at -5 - 20℃; for 0.333333h;Reflux; 6.02.04.37 5-bromo-3-phenyl-lH-(l, 2, 4) triazole 115 mL bromine hydro acid was added to 9.5 g 5-phenyl-2H-(l, 2, 4) triazol-3-ylamine and 12.3 g sodiumnitrite at -5°C. The reaction was warmed to RT and refluxed for 20 min. Then the mixture was cooled and basicfied with sodiumdicarbonate and extracted with ethyl acetate. The organic layer was dried and evaporated to give 11 g of the desired product. Rt: 1.07 min (method B), (M+H)+: 223/225
11 g With hydrogen bromide; sodium nitrite; at -5 - 20℃; for 0.333333h;Reflux; 6.02.04.37 5-bromo-3-phenyl-1H-(1,2,4)triazole 115 mL bromine hydro acid was added to 9.5 g <strong>[4922-98-9]5-phenyl-2H-(1,2,4)triazol-3-ylamine</strong> and 12.3 g sodiumnitrite at -5° C. The reaction was warmed to RT and refluxed for 20 min. Then the mixture was cooled and basicfied with sodiumdicarbonate and extracted with ethyl acetate. The organic layer was dried and evaporated to give 11 g of the desired product. Rt: 1.07 min (method B), (M+H)+: 223/225 By using the same synthesis strategy as for 5-bromo-3-phenyl-1H-(1,2,4)triazole the following compound was obtained:
 

Historical Records

Technical Information

Categories