ChemicalBook Product Catalog Chemical Reagents Organic reagents Halogenated aliphatic hydrocarbons 2-(Trifluoromethyl)acrylic acid

2-(Trifluoromethyl)acrylic acid

2-(Trifluoromethyl)acrylic acid Basic information
Product Name:2-(Trifluoromethyl)acrylic acid
Synonyms:2-(Trifluoromethyl)propenoicacid,min.98%;2-(Trifluoromethyl)propenoic acid 98%;2-(Trifluoromethyl)propenoicacid98%;TRIFLUOROMETHYLACRYLIC ACID;2-(TRIFLUOROMETHYL)ACRYLIC ACID 98%;2-(TRIFLUOROMETHYL)PROPENOIC ACID;2-(TRIFLUOROMETHYL)ACRYLIC ACID;2-(Trifluoromethyl)acrylic acid(98%)
CAS:381-98-6
MF:C4H3F3O2
MW:140.06
EINECS:
Product Categories:pharmacetical;Fluorochemicals;Fluorinated Building Blocks;Fluorinating Reagents & Building Blocks for Fluorinated Biochemical Compounds;Synthetic Organic Chemistry;Acrylic Acids and SaltsSelf Assembly&Contact Printing;Acrylic Monomers;Fluorine-Containing Monomers for 157 nm UV Lithography Resist Polymers;Lithography Monomers;Monomers
Mol File:381-98-6.mol
2-(Trifluoromethyl)acrylic acid Structure
2-(Trifluoromethyl)acrylic acid Chemical Properties
Melting point 51-52 °C (lit.)
Boiling point 86 °C
density 1.3949 (estimate)
Fp 179 °F
storage temp. 2-8°C
pka2.07±0.11(Predicted)
form Chunks
color Light yellow
Water Solubility Soluble in water.
InChIKeyVLSRKCIBHNJFHA-UHFFFAOYSA-N
CAS DataBase Reference381-98-6(CAS DataBase Reference)
Safety Information
Hazard Codes C,Xi
Risk Statements 34-36/37/38
Safety Statements 26-36/37/39-45-37/39
RIDADR UN 3261 8/PG 2
WGK Germany 3
Hazard Note Corrosive
HazardClass 8
PackingGroup III
HS Code 29161900
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
2-(Trifluoromethyl)acrylic acid Usage And Synthesis
Chemical PropertiesLIGHT YELLOW TRANSPARENT CHUNKS
Uses2-(Trifluoromethyl)acrylic acid is used as an acidic functional monomer for molecular imprinting of nicotine. And also used in the conventional functional monomer methacrylic acid.
Uses2-(Trifluoromethyl)acrylic acid (TFMAA) is a strong acid functional monomer, which shows a good performance in the solid-phase extraction of domoic acid. It can also be used in the preparation of molecularly imprinted polymers that show diastereoselectivity for cinchona alkaloids.
Poly(methyl methacrylate) Ethyl 2-(Chlorosulfonyl)acetate Methyl propiolate Butyl methacrylate Acrylic Fiber 2-Hydroxyethyl methacrylate Folic acid POLYMETHACRYLATE Glycine Trifluoromethyl 2-(Trifluoromethyl)acrylic acid Acrylic acid phosphoric acid ETHOXYLATED BISPHENOL A DIACRYLATE Poly(acrylic acid) Methyl methacrylate Methacrylic acid Ethyl methacrylate
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