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2,4,6-Triisopropylbenzoic acid, 97%
CAS: 49623-71-4 | C16H24O2 | 248.366 g/mol
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化學識別
CAS49623-71-4
IUPAC Name2,4,6-tris(propan-2-yl)benzoic acid
Molecular FormulaC16H24O2
InChI KeyULVHAZFBJJXIDO-UHFFFAOYSA-N
SMILESCC(C)C1=CC(C(C)C)=C(C(O)=O)C(=C1)C(C)C
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規格
規格表
規格表Assay (Aqueous acid-base Titration)≥98.0 to ≤102.0%
Identification (FTIR)Conforms
Appearance (Color)White to cream or pale yellow or pale brown
Water Content (Karl Fischer Titration)≤1.5%
FormCrystals or powder or crystalline powder
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2,4,6-Triisopropylbenzoic acid is a hindered acid intermediate compound in organic synthesis.
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
2,4,6-Triisopropylbenzoic acid is a hindered acid intermediate compound in organic synthesis.
Solubility
Slightly soluble in water.
Notes
Store in cool, dry conditions in a well sealed container. Store away from oxidizing agents.
2,4,6-Triisopropylbenzoic acid is a hindered acid intermediate compound in organic synthesis.
Solubility
Slightly soluble in water.
Notes
Store in cool, dry conditions in a well sealed container. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Rainer Schlecker; Dieter Seebach; and Winfried Lubosch. CH-Acidität in α-Stellung zum N-Atom in N,N-dialkylamiden mit sterisch geschützter Carbonylgruppe zur nucleophilen minoalkylierung. Helvetica Chimica Acta. 1978, 61 (1), 512-526.
- Adelina Voutchkova; Abigail Coplin; Nicholas E. Leadbeater and Robert H. Crabtree. Palladium-catalyzed decarboxylative coupling of aromatic acids with aryl halides or unactivated arenes using microwave heating. Chem. Commun. 2008, (47), 6312-6314.
- Hindered acid.