Home Cart Sign in  
Chemical Structure| 1235451-65-6 Chemical Structure| 1235451-65-6

Structure of 1235451-65-6

Chemical Structure| 1235451-65-6

*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 [ 1235451-65-6 ]

CAS No. :1235451-65-6
Formula : C8H9Br2NO
M.W : 294.97
SMILES Code : NC1=CC(Br)=CC=C1OCCBr

Safety of [ 1235451-65-6 ]

Application In Synthesis of [ 1235451-65-6 ]

* 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 [ 1235451-65-6 ]

[ 1235451-65-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1235451-65-6 ]
  • [ 105655-01-4 ]
YieldReaction ConditionsOperation in experiment
94% With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 4h; A mixture of the product 5-bromo-2-(2-bromoethoxy)benzenamine (250 mg, 0.848 mmol) and K2C03 (234 mg, 1.695 mmol) in DMF (5 mL) was stirred at 60 C for 4 h. The mixture was diluted with water (100 mL) and extracted with ethyl acetate (100 mL). The organic layer was washed with water (3 x 50 mL) and brine (50 mL), concentrated to give 6-bromo-3,4-dihydro-2H-benzo[6][l,4]oxazine (170 mg, 94%) as a yellow oil. LCMS: 214 [M+l]+. 1H NMR (400 MHz, DMSO-<¾) delta 3.26 (m, 2H), 4.08 (t, J= 4.8 Hz, 2H), 6.06 (s, 1H), 6.56 (m, 2H), 6.69 (d, J= 1.6 Hz, 1H).
94% With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 4h; A mixture of the product 5-bromo-2-(2-bromoethoxy)benzenamine (250 mg, 0.848 mmol) and K2CO3 (234 mg, 1.695 mmol) in DMF (5 mL) was stirred at 60 C. for 4 h. The mixture was diluted with water (100 mL) and extracted with ethyl acetate (100 mL). The organic layer was washed with water (3×50 mL) and brine (50 mL), concentrated to give 6-bromo-3,4-dihydro-2H-benzo[b][1,4]oxazine (170 mg, 94%) as a yellow oil. LCMS: 214 [M+1]+. 1H NMR (400 MHz, DMSO-d6) delta 3.26 (m, 2H), 4.08 (t, J=4.8 Hz, 2H), 6.06 (s, 1H), 6.56 (m, 2H), 6.69 (d, J=1.6 Hz, 1H)
94% With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 4h; The product 5-bromo-2- (2-bromoethoxy) benzene amine (250mg, 0.848mmol) and K2CO3 (234mg, 1.695mmol) A mixture of in DMF (5 mL), and stirred for 4 hours at 60 C.. The mixture was diluted with water (100 mL), and extracted with ethyl acetate (100 mL). The organic layer was washed with water (3 × 50 mL) and brine (50 mL), concentrated to give 6-bromo-3,4-dihydro -2H- benzo [b] [1,4] oxazine as a yellow oil (170 mg , 94%).
 

Historical Records

Technical Information

Categories