4-(Trifluoromethylsulfonyl)phenylacetic acid, 98%, Thermo Scientific Chemicals
Element SearchElement SearchStructure SearchStructure Search
4-(Trifluoromethylsulfonyl)phenylacetic acid, 98%, Thermo Scientific Chemicals
4-(Trifluoromethylsulfonyl)phenylacetic acid, 98%, Thermo Scientific Chemicals
4-(Trifluoromethylsulfonyl)phenylacetic acid, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-(Trifluoromethylsulfonyl)phenylacetic acid, 98%, Thermo Scientific Chemicals

CAS: 1099597-82-6 | C9H7F3O4S | 268.206 g/mol
Have Questions?
Catalog NumberQuantity
ALFH32295.031 g
Catalog number ALFH32295.03
View Price:Sign in to see your account pricing. Need an account? Register with us today.
Quantity:
1 g
Request bulk or custom format
Chemical Identifiers
CAS7440-02-0
IUPAC Namenickel
Molecular FormulaNi
InChI KeyPXHVJJICTQNCMI-UHFFFAOYSA-N
SMILES[Ni]
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Form)Powder
Total trace metal impurities=<0.1 %
Particle size=<44 µm
Appearance (Color)Grey
4-(Trifluoromethylsulfonyl)phenylacetic acid, is used as a primary and secondary intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-(Trifluoromethylsulfonyl)phenylacetic acid, is used as a primary and secondary intermediate.

Solubility
Slightly soluble in water, soluble in organic solvents.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. A Aramini.; MR Sablone.; G Bianchini.; A Amore.;M Fanì. Facile one-pot preparation of 2-arylpropionic and arylacetic acids from cyanohydrins by treatment with aqueous HI. Tetrahedron..200965 (10), 2015-2021.
  2. E Valeur.; M Bradley. Amide bond formation: beyond the myth of coupling reagents. Chemical Society Reviews.200938 (1), 606-631.