1,3-difluoro-2-methylbenzene

Synonym
Product Category
Product Code
CAS Number
MDL Number
Pubchem CID
Reaxys RN
2,6-difluorotoluene
Fluorinated Building Blocks
KUMI2F106
443-84-5
MFCD00043898
581493
1932656
Chemical Name
Molecular Formula
Molecular Weight
Assay(Analysis Method)
Appearance
Boiling Point
Packaging
Storage
1,3-difluoro-2-methylbenzene
C7H6F2
128.12
≥99%(GC)
Colorless Liquid
111-112°C
5g,10g,50g,100g,200g and 500g
Store at 2-8°C temperature
1,3-difluoro-2-methylbenzene is used to generate benzyne radical cations (2,6-difluorobenzyl radical cation) for the synthesis of the corresponding compounds, e.g. benzaldehyde.
Methyl Group Internal Rotation in 2,6-Difluorotoluene (S1) and 2,6-Difluorotoluene+ (D0). [1]
Preparation of 2,6-difluoro-n-alkylbenzenes from 1,3-difluorobenzene Transformation of 2,6-difluorotoluene to the corresponding benzaldehyde via benzyl chloride. [2]
Observation of Vibronic Emission Spectrum of the Jet-Cooled 2,6-Difluorobenzyl Radical. [3]
Effects of Aromatic Substitutions on the Photoreactions in Mg•+(C6HnF2X4-n) (X = F, CH3) Complexes:  Formation and Decomposition of Benzyne Radical Cations. [4]
References:
[1] R.A.Walker, et al, J. Phys. Chem., 1995, 99(33), pp 12422-12433.
[2] E.V.Malykhin, et al, J. F. Chem., 1998, 91(1), pp 12-20.
[3] S.K.Lee, et al, J. Phys. Chem. A, 2000, 104(22), pp 5219-5221.
[4] H.Liu, et al, J. Phys. Chem. A., 2004, 108(16), pp 3356-3366.
Signal Word
Hazard Statements
Precautionary Statements
HS Code
RIDADR
Legal Information
Danger
H225
P210
2903998090
UN 1993 3/PG II

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