| Identification | More | [Name]
3-FLUORO-4-METHYLANISOLE | [CAS]
405-06-1 | [Synonyms]
3-FLUORO-4-METHYLANISOLE
2-Fluoro-4-methoxytoluene
3-Fluoro-4-methylanisole 99%
3-Fluoro-4-methylanisole99%
1-Fluoro-3-methoxy-6-methylbenzene，2-Fluoro-4-methoxytoluene | [Molecular Formula]
C8H9FO | [MDL Number]
MFCD00143163 | [Molecular Weight]
140.15 | [MOL File]
405-06-1.mol |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P280a-P304+P340-P305+P351+P338-P405-P501a | [Hazard Codes ]
F | [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:Wear suitable protective clothing . | [Hazard Note ]
Flammable | [HS Code ]
2909309090 |
| Hazard Information | Back Directory | [Reactions]
3-Fluoro-4-methylanisole is a nucleophilic, ring substituted electron acceptor that can be activated by electron donors. The nitro group and the electron donating substituents on the ring are important for this reactivity. 3-Fluoro-4-methylanisole can form substitution products with methyl or formyl groups in the presence of a strong base such as palladium, 3-fluoro-4-methylphenol, or nitro groups. This reactivity is regiospecific, meaning that the substitution will only occur at one of two possible sites on the ring. 3-Fluoro-4-methylanisole's chemical properties give it both activating and deactivating properties in organic reactions. |
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