| Identification | More | [Name]
2-Fluoro-3-methylpyridine | [CAS]
2369-18-8 | [Synonyms]
2-FLUORO-3-METHYLPYRIDINE
2-FLUORO-3-PICOLINE
2-FLUORO-3-METHYLPYRIDINE 97%
2-Fluoro-3-methylpyridine98%
2-FLUORO-3-METHYLPYRIDINE (2-FLUORO-3-PICOLINE)
2-Fluoro-3-methyl pyridine ,97% | [EINECS(EC#)]
624-901-9 | [Molecular Formula]
C6H6FN | [MDL Number]
MFCD00041223 | [Molecular Weight]
111.12 | [MOL File]
2369-18-8.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless to light yellow liquid | [Boiling point ]
154-155 °C (lit.) | [density ]
1.098 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.476(lit.)
| [Fp ]
119 °F
| [storage temp. ]
Flammables area | [pka]
-0.14±0.10(Predicted) | [Specific Gravity]
1.098 | [Detection Methods]
GC | [BRN ]
1877 | [CAS DataBase Reference]
2369-18-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,F,Xn | [Risk Statements ]
R10:Flammable.
R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S16:Keep away from sources of ignition-No smoking . | [RIDADR ]
UN 1993 3/PG 3
| [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT, FLAMMABLE | [PackingGroup ]
Ⅲ | [HS Code ]
29333990 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless to light yellow liquid | [Uses]
2-Fluoro-3-methylpyridine may be used in the preparation of:
- 2-phenyl-3-methylpyridine
- 2-(4-chlorophenyl)-3-methylpyridine
- 2-(4-fluorophenyl)-3-methylpyridine
- 2-fluoronicotinic acid
| [General Description]
2-Fluoro-3-methylpyridine, also known as 2-fluoro-3-picoline, can be prepared by reacting 2-amino-3-methylpyridine and 40% fluoroboric acid.2 The signs of the long range coupling constants of 2-fluoro-3-methylpyridine have been obtained by double and triple resonance techniques. |
|
|