2-methyl-5-(trifluoromethyl)furan

Synonym
Product Category
Product Code
CAS Number
MDL Number
Pubchem CID
Reaxys RN
5-trifluoromethyl-2-methylfuran
Trifluoromethyl Building Blocks
KUMI3F83
17515-75-2
MFCD08437602
10953688
7700749
image-155171-Trimethyl(trifluoromethyl)silane_reagent.png
Chemical Name
Molecular Formula
Molecular Weight
Assay
Appearance
Boiling Point
Packaging
Storage
2-methyl-5-(trifluoromethyl)furan
C6H5F3O
150.10
≥98.0%(GC)
Liquid
80-85°C
1g,5g,10g,25g,50g,100g and 500g
Store at room temperature
2-methyl-5-(trifluoromethyl)furan is an important trifluoromethylated heterocycle building block for the synthesis of various pharmaceutical products, agrochemicals and are widely applied in material sciences.
Reaction of ethyl 4,4,4-trifluoroacetoacetate enolate with 3-bromo-1,1,1-trifluoroacetone: Synthesis of 2,4-bis (trifluoromethyl) furan. [1]
Silver-catalysed trifluoromethylation of arenes at room temperature. [2]
Rapid trifluoromethylation and perfluoroalkylation of five-membered heterocycles by photoredox catalysis in continuous flow. [3]
References:
[1] J.Q.Smith, et al, J. F. Chem., 1997, 81(2), pp 123-128.
[2] S.Seo, et al, Chem. Commun., 2013, 49(57), pp 6385-6387.
[3] N.J.W.Straathof, et al, ChemSuschem, 2014, 7(6), pp 1612-1617.
Signal Word
Hazard Statements
Precautionary Statements
HS Code
RIDADR
Legal Information
Warning
H315,H319,H335
P264,P302+P352,P305+P351+P338

NONH for all modes of transport

1. Product Specification
2. Safety Data Sheet
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