ChemicalBook--->CAS DataBase List--->74356-36-8

74356-36-8

74356-36-8 Structure

74356-36-8 Structure
IdentificationBack Directory
[Name]

2,4-DIMETHYL-PYRIMIDINE-5-CARBOXYLIC ACID
[CAS]

74356-36-8
[Synonyms]

ASISCHEM C71549
TIMTEC-BB SBB010333
CHEMBRDG-BB 4019260
ASINEX-REAG BAS 07567148
2,4-dimethylpyrimidine-5-carboxylicaci
2,4-dimethyl-5-pyrimidinecarboxylic acid
2,4-DIMETHYL-PYRIMIDINE-5-CARBOXYLIC ACID
5-Pyrimidinecarboxylicacid,2,4-dimethyl-(6CI,9CI)
2,4-dimethylpyrimidine-5-carboxylic acid(SALTDATA: FREE)
2,4-DIMETHYL-PYRIMIDINE-5-CARBOXYLIC ACID ISO 9001:2015 REACH
[Molecular Formula]

C7H8N2O2
[MDL Number]

MFCD07391755
[MOL File]

74356-36-8.mol
[Molecular Weight]

152.15
Chemical PropertiesBack Directory
[Melting point ]

154-155 °C(Solv: ethyl acetate (141-78-6))
[Boiling point ]

299.6±20.0 °C(Predicted)
[density ]

1.257±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

2.62±0.25(Predicted)
[Appearance]

White to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[HazardClass ]

IRRITANT
Raw materials And Preparation ProductsBack Directory
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-DIMETHYL-PYRIMIDINE-5-CARBOXYLIC ACID(74356-36-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

ETHYL-2,4-DIMETHYL-5-PYRIMIDINE CARBOXYLATE

2226-86-0

2,4-DIMETHYL-PYRIMIDINE-5-CARBOXYLIC ACID

74356-36-8

The general procedure for the synthesis of 2,4-dimethylpyrimidine-5-carboxylic acid from ethyl 2,4-dimethylpyrimidine-5-carboxylate was as follows: potassium hydroxide (67 g, 1.0 mol) was dissolved in 95% ethanol (300 mL), and this solution was then added to a 95% ethanol (100 mL) solution of ethyl 2,4-dimethyl-5-pyrimidinecarboxylate (73 g, 0.40 mol) to the solution. The mixture was heated under reflux conditions for 5 hours. Upon completion of the reaction, the ethanol was removed by evaporation under reduced pressure, the residue was dissolved in water and the aqueous solution was acidified with concentrated hydrochloric acid. The precipitated solid was collected by filtration, washed with water and dried to give 2,4-dimethylpyrimidine-5-carboxylic acid (36 g, 58% yield). The product was characterized by 1H-NMR (CDCl3), δ: 2.63 (3H, s), 2.69 (3H, s), 8.97 (1H, s).

[References]

[1] Journal of Heterocyclic Chemistry, 1990, vol. 27, # 2, p. 295 - 305
[2] Patent: EP1402900, 2004, A1
[3] Patent: EP1364949, 2003, A1. Location in patent: Page/Page column 100
[4] Chemistry of Heterocyclic Compounds, 2007, vol. 43, # 11, p. 1479 - 1480
[5] Patent: EP2019099, 2009, A1. Location in patent: Page/Page column 15-16
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