| Identification | More | [Name]
3-METHYL-4-PYRIDINECARBOXYLIC ACID | [CAS]
4021-12-9 | [Synonyms]
3-METHYL-4-PYRIDINECARBOXYLIC ACID
3-METHYL-4-PYRIDINYLCARBOXIC ACID
3-METHYL-ISONICOTINIC ACID
3-METHYLPYRIDINE-4-CARBOXYLIC ACID
ASINEX-REAG BAS 07668195
3-Methyl-4-pyridinecarboxylic acid ,97% | [Molecular Formula]
C7H7NO2 | [MDL Number]
MFCD00128870 | [Molecular Weight]
137.14 | [MOL File]
4021-12-9.mol |
| Chemical Properties | Back Directory | [Melting point ]
235℃ | [Boiling point ]
389℃ | [density ]
1.230 | [Fp ]
189℃ | [storage temp. ]
Inert atmosphere,Room Temperature | [pka]
0.82±0.25(Predicted) | [Appearance]
White to light yellow Solid | [Detection Methods]
HPLC | [InChI]
InChI=1S/C7H7NO2/c1-5-4-8-3-2-6(5)7(9)10/h2-4H,1H3,(H,9,10) | [InChIKey]
OSMAGAVKVRGYGR-UHFFFAOYSA-N | [SMILES]
C1=NC=CC(C(O)=O)=C1C | [CAS DataBase Reference]
4021-12-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [HazardClass ]
IRRITANT | [HS Code ]
2933399990 |
| Hazard Information | Back Directory | [Uses]
3-Methyl-4-pyridinecarboxylic acid can be used in the preparation of 4,5-dihydro-1H-pyrazole derivatives as cholesterol 24 hydroxylase inhibitors for prevention and/or treatment of neurodegenerative disease.
| [Uses]
An Isonicotinic Acid (I821760) derivative. Used in the preparation of 4,5-dihydro-1H-pyrazole derivatives as cholesterol 24 hydroxylase inhibitors for prevention and/or treatment of neurodegenerative disease. | [Synthesis]
The general procedure for the synthesis of 3-methyl-4-pyridinecarboxylic acid from 3,4-dimethylpyridine was as follows: 3,4-dimethylpyridine (119.30 g, 0.28 mol) was dissolved in diphenyl ether (150 mL) and heated to 150-170 °C, followed by the slow addition of selenium dioxide (62 g, 0.56 mol). Selenium dioxide was added in batches over a period of 1 hour. The reaction mixture was heated to 180 °C and maintained at this temperature for 1 hour. Upon completion of the reaction, the mixture was filtered while hot and the collected precipitate was washed with boiling water (3 x 300 mL). The filtrates were combined and extracted with chloroform (3 x 300 mL). The aqueous phase was evaporated to dryness and the resulting crude product was recrystallized from ethanol (450 mL) to give pure 3-methyl-4-pyridinecarboxylic acid (18 g, 47% yield) with a melting point of 220-222°C (Literature value: J. Chem. Soc., Perkin Trans. 1, 1984, 1501-1505, melting point 232°C).1H NMR (300 MHz, DMSO-d6) δ 8.59 (s, 1H), 8.04 (s, 1H), 8.47 (d, J = 4.8 Hz, 1H), 7.69 (d, J = 4.8 Hz, 1H), 2.48 (s, 3H). | [References]
[1] Journal of Medicinal Chemistry, 2012, vol. 55, # 4, p. 1682 - 1697
[2] Patent: US2014/18360, 2014, A1. Location in patent: Paragraph 0152
[3] Journal of Medicinal Chemistry, 2012, vol. 55, # 22, p. 10118 - 10129
[4] Patent: US5952343, 1999, A
[5] Patent: US5461154, 1995, A |
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