Home Cart Sign in  
Chemical Structure| 20294-59-1 Chemical Structure| 20294-59-1

Structure of 20294-59-1

Chemical Structure| 20294-59-1

*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 [ 20294-59-1 ]

CAS No. :20294-59-1
Formula : C10H12BrNO3
M.W : 274.11
SMILES Code : OC1=C(C(C)(C)C)C=C([N+]([O-])=O)C=C1Br

Safety of [ 20294-59-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H315-H317-H318-H410
Precautionary Statements:P261-P264-P270-P272-P273-P280-P301+P312+P330-P302+P352-P305+P351+P338+P310-P333+P313-P391-P501
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 20294-59-1 ]

* 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 [ 20294-59-1 ]

[ 20294-59-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6683-81-4 ]
  • [ 20294-59-1 ]
YieldReaction ConditionsOperation in experiment
100% With pyridinium hydrobromide perbromide; acetic acid; at 20℃; for 5h; Part F. Preparation of 2-bromo-6-tert-butyl-4-nitrophenol.; [00756] A solution of the product from Part E (l.Og, 5.12mmol) in glacial acetic acid (10.25mL) was treated portion wise with pyridine hydrobromide perbromide (1.8Og, 5.63mmol) followed by stirring at room temperature for 2h. Additional pyridinium hydrobromide perbromide (3.6g) was added in two portions and after another 3h of stirring, the reaction was complete. The mixture was poured into ice water, and the mixture treated with a small amount of sodium sulfite. The resulting solid was filtered and dried under vacuum to give the title compound as a brown solid (1.4Og, 100 %).
100% With pyridinium perbromide hydrobromide; acetic acid; at 20℃; for 5h; [00498] Part F. Preparation of 2-bromo-6-tert-butyl-4-nitrophenol.; [00499] A solution of the product from Part E (l.Og, 5.12mmol) in glacial acetic acid (10.25mL) was treated portion wise with pyridine hydrobromide perbromide (1.8Og, 5.63mmol) followed by stirring at room temperature for 2h. Additional pyridinium hydrobromide perbromide (3.6g) was added in two portions and after another 3h of stirring, the reaction was complete. The mixture was poured into ice water, and the mixture treated with a small amount of sodium sulfite. The resulting solid was filtered and dried under vacuum to give the title compound as a brown solid (1.4Og, 100 %).
100% With pyridinium hydrobromide perbromide; acetic acid; at 20℃; for 5h; Part D. Preparation of 2-bromo-6-tert-butyl-4-nitrophenol.; [00595] A solution of the product from Part C (l.Og, 5.12mmol) in glacial acetic acid (10.25mL) was treated portion wise with pyridine hydrobromide perbromide (1.8Og, 5.63mmol) followed by stirring at room temperature for 2h. Additional pyridinium hydrobromide perbromide (3.6g) was added in two portions and after another 3h of stirring, the reaction was complete. The mixture was poured into ice water, and the mixture treated with a small amount of sodium sulfite. The resulting solid was filtered and dried under vacuum to give the title compound as a brown solid (1.4Og, 100 %).
 

Historical Records

Technical Information

Categories