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ChemicalBook--->CAS DataBase List--->405-06-1

405-06-1

405-06-1 Structure

405-06-1 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[Boiling point ]

63.5-64°C
[density ]

1.046±0.06 g/cm3(Predicted)
[refractive index ]

1.4909
[storage temp. ]

Sealed in dry,Room Temperature
[CAS DataBase Reference]

405-06-1(CAS DataBase Reference)
Safety DataBack 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 InformationBack 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.
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

405-06-1(sigmaaldrich)
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