Home Cart Sign in  
Chemical Structure| 192650-54-7 Chemical Structure| 192650-54-7

Structure of 192650-54-7

Chemical Structure| 192650-54-7

*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 [ 192650-54-7 ]

CAS No. :192650-54-7
Formula : C9H10FNO2
M.W : 183.18
SMILES Code : O=C(OC)CC1=CC=C(N)C=C1F
MDL No. :MFCD20727501

Safety of [ 192650-54-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 192650-54-7 ]

* 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 [ 192650-54-7 ]

[ 192650-54-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 337529-74-5 ]
  • [ 192650-54-7 ]
YieldReaction ConditionsOperation in experiment
86% With palladium on activated charcoal; hydrogen; In ethyl acetate; for 5h; To a 50 ml round bottom flask, were added <strong>[337529-74-5]methyl 2-(2-fluoro-4-nitrophenyl)acetate</strong> (3.8 g, 0.018 mol) and ethyl acetate (30 ml). To the same flask, 10 percent palladium on activated carbon (0.5 g) was added. The reaction mixture was stirred under hydrogen gas (using bladder) atmosphere for 5 h. The reaction mixture was filtered through a pad of celite. The filtrate was evaporated under reduced pressure to get the title compound (2.8 g, 86%), MS (+) ES: 184 (M+H)+.
With palladium 10% on activated carbon; hydrogen; In methanol; In a 50 mL round-bottomed flask 20 (300 mg, 1.4 mmol) was dissolved in MeOH (10 mL) and Pd/C (10%, 75 mg) was added and the mixture hydrogenated with a hydrogen balloon overnight. The mixture was filtered, and evaporated to afford the title compound T-21 quantatively as a reddish oil which was used without further purification.
 

Historical Records

Technical Information

Categories