Home Cart Sign in  
Chemical Structure| 1053656-65-7 Chemical Structure| 1053656-65-7

Structure of 1053656-65-7

Chemical Structure| 1053656-65-7

*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 [ 1053656-65-7 ]

CAS No. :1053656-65-7
Formula : C10H12FNO2
M.W : 197.21
SMILES Code : O=C(OC(C)(C)C)C1=NC(F)=CC=C1
MDL No. :MFCD10568316
InChI Key :HUSBMKLNFMAIMJ-UHFFFAOYSA-N
Pubchem ID :46835593

Safety of [ 1053656-65-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-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 [ 1053656-65-7 ]

* 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 [ 1053656-65-7 ]

[ 1053656-65-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 402-69-7 ]
  • [ 75-65-0 ]
  • [ 1053656-65-7 ]
YieldReaction ConditionsOperation in experiment
83% With pyridine; p-toluenesulfonyl chloride; at 0 - 20℃; for 12h; Tosyl chloride (915 mg, 4.8 mmol) was added to a solution of 2-fiuoro- picolinic acid (254 mg, 2 mmol) and pyridine (1.08 mL, 13.4 mmol) in 3.6 mL of t-BuOH at 00C. The reaction was then stirred at room temperature for 12 hours. An aqueous solution of NaHCO3 was then added and the mixture was extracted with ethyl acetate (3 times). The combined organic phases were washed with brine and dried over Na2SO4. The crude compound was purified by flash chromatography using SiO2 (Petroleum Ether/EtOAc 100:0 to 90: 10). The product 120A was obtained as a white solid (m = 326 mg, 83percent): 1H NMR (ppm, CDCl3) 1.6 (s, 9H), 7.05-7.11 (m, IH), 7.85-7.93 (m, 2H).
 

Historical Records

Technical Information

Categories