Home Cart Sign in  
Chemical Structure| 59237-49-9 Chemical Structure| 59237-49-9

Structure of 59237-49-9

Chemical Structure| 59237-49-9

*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 [ 59237-49-9 ]

CAS No. :59237-49-9
Formula : C8H8N2O5
M.W : 212.16
SMILES Code : O=C(OC)C1=CN=C(OC)C([N+]([O-])=O)=C1
MDL No. :MFCD02090529

Safety of [ 59237-49-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 59237-49-9 ]

* 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 [ 59237-49-9 ]

[ 59237-49-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 59237-53-5 ]
  • [ 166742-22-9 ]
  • [ 59237-49-9 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate; In methanol; water; sodium thiomethoxide; REFERENCE EXAMPLE 44 A solution of sodium methoxide in methanol (82.65 ML; 1 M) is added slowly to a stirred solution of <strong>[59237-53-5]methyl 6-chloro-5-nitronicotinate</strong> (17 g) in anhydrous methanol (250 ML) and the mixture is stirred for 8 hours. The mixture is concentrated, and the residue is treated with water and extracted with ethyl acetate. The extract is washed with water, treated with decolourising charcoal, and dried over magnesium sulphate. Concentration gives methyl 6-methoxy-5-nitronicotinate (9.8 g), in the form of an orange solid. Recrystallization from cyclohexane gives white needles, m.p.118-119°C. By proceeding in a similar manner using sodium thiomethoxide instead of sodium methoxide as the starting material, there is prepared methyl 6-methylthio-5-nitronicotinate.
  • 2
  • [ 59237-53-5 ]
  • [ 59237-49-9 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate; In methanol; water; REFERENCE EXAMPLE 17 Sodium methoxide in methanol (82.65 mL of a 1 M solution) is added slowly to a stirred solution of <strong>[59237-53-5]methyl 6-chloro-5-nitronicotinate</strong> (17 g) in anhydrous methanol (250 mL) and the mixture stirred for 8 hours. The mixture is concentrated, the residue treated with water and then extracted into ethyl acetate. The extracts are washed with water, treated with decolourising charcoal and dried (MgSO4). Concentration afforded methyl 6-methoxy-5-nitronicotinate (9.8 g) as an orange solid. Recrstallisation from cyclohexane afforded white needles, m.p.118-9° C.
  • 3
  • [ 59237-53-5 ]
  • [ 124-41-4 ]
  • [ 59237-49-9 ]
YieldReaction ConditionsOperation in experiment
95% In methanol; b)Methyl 6-methoxy-5-nitronicotinateSodium methoxide (2.1 g, 38.9 mmol) was added portionwise to a stirred suspension of <strong>[59237-53-5]methyl 6-chloro-5-nitronicotinate</strong> (Preparation 9a, 2.86 g, 13.21 mmol) in anhydrous methanol (45 mL) and the mixture was stirred overnight.The mixture was concentrated and the residue was partitioned between ethyl acetate and water and the organic layer was washed with brine, dried (MgSO4 and evaporated to give the title compound (2.66 g, 95percent) as a cream-coloured solid.LRMS (m/z): 217 (M+1)+.1H NMR delta (300 MHz, CDCl3): 3.98 (s, 3H), 4.20 (s, 3H), 8.83 (d, 1H), 9.01 (d, 1H).
In methanol; b) Methyl 6-methoxy-5-nitronicotinateSodium methoxide (2.1 g, 38.9 mmol) was added portion wise to a stirred suspension of <strong>[59237-53-5]methyl 6-chloro-5-nitronicotinate</strong> (Preparation 9a, 2.86 g, 13.21 mmol) in anhydrous methanol (45 mL) and the mixture was stirred overnight. The mixture was concentrated and the residue was partitioned between ethyl acetate and water and the organic layer was washed with brine, dried (MgS04) and evaporated to give the title compound (2.66 g, 95percent) as a cream-coloured solid.LRMS (m/z): 217 (M+1 )+.1H NMR delta (300 MHz, CDCI3): 3.98 (s, 3H), 4.20 (s, 3H), 8.83 (d, 1 H), 9.01 (d,1 H).
 

Historical Records

Technical Information

Categories