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Thermo Scientific Chemicals
4-(Trifluoromethylsulfonyl)phenylacetic acid, 98%
CAS: 1099597-82-6 | C9H7F3O4S | 268.206 g/mol
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Catalog number H32295.03
also known as H32295-03
Price (EUR)
108,00
Each
Quantity:
1 g
Price (EUR)
108,00
Each
Chemical Identifiers
CAS1099597-82-6
IUPAC Name2-(4-trifluoromethanesulfonylphenyl)acetic acid
Molecular FormulaC9H7F3O4S
InChI KeyFIEUCHICQSJBAU-UHFFFAOYSA-N
SMILESOC(=O)CC1=CC=C(C=C1)S(=O)(=O)C(F)(F)F
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White
Assay (HPLC)≥97.5%
FormCrystals or powder or crystalline powder
Melting Point (clear melt)123.0-129.0?C
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
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.
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:
- 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.
- E Valeur.; M Bradley. Amide bond formation: beyond the myth of coupling reagents. Chemical Society Reviews.200938 (1), 606-631.