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Chemical Structure| 612088-38-7 Chemical Structure| 612088-38-7

Structure of 612088-38-7

Chemical Structure| 612088-38-7

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Product Details of [ 612088-38-7 ]

CAS No. :612088-38-7
Formula : C7H6N2O4
M.W : 182.14
SMILES Code : O=C(O)C1=NC=NC(C(OC)=O)=C1
MDL No. :N/A
InChI Key :LHMRMRJXNBERPE-UHFFFAOYSA-N
Pubchem ID :58686018

Safety of [ 612088-38-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 612088-38-7 ]

* 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 [ 612088-38-7 ]

[ 612088-38-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6345-43-3 ]
  • [ 612088-38-7 ]
YieldReaction ConditionsOperation in experiment
Ca. 100% With water; sodium hydroxide; In methanol; at 0 - 20℃; for 2h; Sodium hydroxide (632 mg, 15.8 mmol) was added to a solution of compound 81-1 (3.10 g, 15.8 mmol) in MeOH (60 mL) and H20 (6 mL) at 0C. The resulting mixture was stirred for 2 h at room temperature, then acidified with 1M HC1 aqueous to pH of 3. The mixture was concentrated to dryness. The residue was azeotroped two times with THF (50 mL portions) to afford crude compound 81-2 (3.30 g, -100% yield), which was used for next step without further purification.
86% With methanol; sodium hydroxide; at 20℃; for 1h;Inert atmosphere; To a 100 ml round bottom flask containing a stir bar is added commercially available pyrimidine-4,6- dicarboxylic acid dimethyl ester (19) (obtained from Aldrich). To the solid was added a solution comprising 0.2 grams of sodium hydroxide dissolved in 10 ml anhydrous methanol and mixture stirred at room temperature under a nitrogen atmosphere for 1 hour. To the reaction mixture was then added 1.2 ml of a solution comprising 4 M hydrochloric acid in dioxane and mixture stirred for 10 minutes. To the reaction mixture was then added ~2 grams of silica gel (Si02), and the volatile components removed under reduced pressure and solid added to a column and purified via column chromatography (Si02, 40% ethylacetate in hexane) to give 0.77 grams (86%) of Pyrimidine-4,6-dicarboxylic acid monomethyl ester compound (20). XH NMR (300 MHz, CD3OD) delta 4.04 (s, 3H), 8.59 (s, 1H), 9.46 (s, 1H). LC-MS (M+H) 183.
76% To a solution of sodium hydroxide (1.00 g) in dry methanol (50 mL) was added commercially available <strong>[6345-43-3]pyrimidine-4,6-dicarboxylic acid dimethyl ester</strong> (4.91 g). The resulting suspension was stirred at room temperature for 1 h. Then a 4M solution of hydrochloric acid in dioxane (6.25 mL) was added and stirring at room temperature was continued for 10 min. The mixture was concentrated and purified by flash chromatography (silica, dichloromethane/methanol) to afford the title compound (3.48 g; 76%). [MH]+=183.
76% Preparative Example 200; Step A; To a solution of sodium hydroxide (1.00 g) in dry methanol (50 mL) was added commercially available <strong>[6345-43-3]pyrimidine-4,6-dicarboxylic acid dimethyl ester</strong> (4.91 g). The resulting suspension was stirred at room temperature for 1 h. Then a 4M solution of hydrochloric acid in dioxane (6.25 mL) was added and stirring at room temperature was continued for 10 min. The mixture was concentrated and purified by flash chromatography (silica, dichloromethane/methanol) to afford the title compound (3.48 g; 76%). [MH]+=183.

  • 2
  • [ 16490-02-1 ]
  • [ 612088-38-7 ]
 

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