Home Cart Sign in  
Chemical Structure| 1253789-63-7 Chemical Structure| 1253789-63-7

Structure of 1253789-63-7

Chemical Structure| 1253789-63-7

*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 [ 1253789-63-7 ]

CAS No. :1253789-63-7
Formula : C7H2ClFN2O2
M.W : 200.55
SMILES Code : N#CC1=C([N+]([O-])=O)C=C(F)C=C1Cl
MDL No. :MFCD17015618

Safety of [ 1253789-63-7 ]

Application In Synthesis of [ 1253789-63-7 ]

* 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 [ 1253789-63-7 ]

[ 1253789-63-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 153505-32-9 ]
  • copper(l) cyanide [ No CAS ]
  • [ 1253789-63-7 ]
YieldReaction ConditionsOperation in experiment
41% Example A; 5a) Preparation of intermediate; Tert-butyl nitrite (25 g, 242 mmol) was added to a suspension of CuCN (21.5 g,242 mmol) in CH3CN (500 ml). The mixture was heated to 70 C and was stirred for 15 min. Subsequently, a mixture of 2-chloro-4-fluoro-6-nitro-benzenamine (23 g,121 mmol) and CH3CN (q.s.) was added, and the resulting brown solution was heated overnight at 70 C. The solvent was removed in vacuo. Water (q.s.) was added to the residue and the aqueous mixture was extracted with EtOAc. The separated organic layer was dried (MgS04), filtered, and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: EtO Ac/petroleum ether 1/4). The desired fractions were collected and the solvent was evaporated. Yield: 10 g of intermediate 10 (41% yield; yellow solid).
41% Tert-butyl nitrite (25 g, 242 mmol) was added to a suspension of CuCN (21.5 g, 242 mmol) in CH3CN (500 ml). The mixture was heated to 70 C. and was stirred for 15 mm. Subsequently, a mixture of 2-chioro-4-fluoro-6-nitro-benze- namine (23 g, 121 mmol) and CH3CN (q.s.) was added, and the resulting brown solution was heated overnight at 70 C. The solvent was removed in vacuo. Water (q.s.) was added to the residue and the aqueous mixture was extracted with EtOAc. The separated organic layer was dried (Mg504), filtered, and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: EtOAc/petroleum ether 1/4). The desired fractions were collected and the solvent was evaporated. Yield: 10 g of intermediate 10 (41% yield; yellow solid).
 

Historical Records