Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 565237-07-2 Chemical Structure| 565237-07-2

Structure of 565237-07-2

Chemical Structure| 565237-07-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 565237-07-2 ]

CAS No. :565237-07-2
Formula : C8H8INO2
M.W : 277.06
SMILES Code : CC(OCC1=NC=CC(I)=C1)=O
English Name :(4-Iodopyridin-2-yl)methyl acetate

Safety of [ 565237-07-2 ]

Application In Synthesis of [ 565237-07-2 ]

* 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 [ 565237-07-2 ]

[ 565237-07-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 565237-08-3 ]
  • [ 75-36-5 ]
  • [ 22282-65-1 ]
  • [ 565237-07-2 ]
YieldReaction ConditionsOperation in experiment
1: 22% 2: 45% With sodium iodide In acetonitrile for 33h; Heating / reflux; 2 4-Iodo-2-methylpyridine and (4-IODO-2-PYRIDYL) methylacetate : 2- ( ( (TETT-BUTYLDIMETHYLSILYL) OXY) METHYL)-4-CHLOROPYRIDINE (600 mg, 2.33 MMOL), dry sodium iodide (5 g) and freshly distilled acetyl chloride (0. 7. mL, 9.78 MMOL) in 6 mL of anhydrous ACETONITRILE were REFLUXED under nitrogen for 33 hours. Aqueous 10% K2CO3/5% NAHSO3 was added and the mixture extracted three times with chloroform. After drying (NA2SO4) and evaporation of the chloroform, flash chromatography (hexane/EtOAc 9 : 1) yielded 110 mg (22%) of 4-Iodo-2- METHYLPYRIDINE as a white solid and 290 mg (45%) of (4-iodo-2-pyridyl) methylacetate as a white solid. 4-Iodo-2-methypyridine: 1H NMR (CHO) 8 8.06 (d, LH, *5. 2 Hz, H-6); 7.48 (d, 1H, J=1.1 Hz, H- 3); 7.38 (dd, 1H, J1=5. 2, 1. 4 Hz, H-5); 2.41 (s, 3H, CH3) ;13C NMR (CDCl3) 8 159.8 (C-2), 149.8 (C-6), 133.0 (C-3), 130.4 (C-5), 106.3 (C-4), 24.5 (CH3). (4-iodo-2-pyridyl) METHYLACETATE : 1H NMR (CDCl3) 8 8.16 (d, 1H, J=5. 2 Hz, H-6); 7.66 (d, LH, J=1. 0 Hz, H-3); 7.54 (dd, 1H, J1=5. 2,. J2=1. 6 Hz, H-5); 5.09 (s, 2H, CH2) ; 2.11 (s, 3H, CH3) ; 13C NMR (CDCTS) 8 170.9 (CO), 157.1 (C-2), 150.1 (C-6), 132.5 (C-3), 131.3 (C-5), 106.6 (C-4), 66.3 (CH2), 21.3 (CH3).
 

Historical Records