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4-Benzoylbenzoic acid, 98%, Thermo Scientific Chemicals
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Catalog number A14993.14
also known as A14993-14
Price (USD)/ Each
271.00
-
Quantity:
25 g
Price (USD)/ Each
271.00
4-Benzoylbenzoic acid, 98%, Thermo Scientific Chemicals
Catalog numberA14993.14
Price (USD)/ Each
271.00
-
Chemical Identifiers
CAS611-95-0
IUPAC Name4-benzoylbenzoic acid
Molecular FormulaC14H10O3
InChI KeyIFQUPKAISSPFTE-UHFFFAOYSA-N
SMILESOC(=O)C1=CC=C(C=C1)C(=O)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale brown
FormPowder or crystalline powder
Assay (Aqueous acid-base Titration)≥98.5 to ≤101.5%
Identification (FTIR)Conforms
Melting Point196-204°C
4-Benzoylbenzoic acid,is a important organic intermediate. It can be used in agrochemical, pharmaceutical and dyestuff field etc.
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-Benzoylbenzoic acid,is a important organic intermediate. It can be used in agrochemical, pharmaceutical and dyestuff field etc.
Solubility
It is soluble in water (partly).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.Incompatible with strong bases, strong oxidizing agents.
4-Benzoylbenzoic acid,is a important organic intermediate. It can be used in agrochemical, pharmaceutical and dyestuff field etc.
Solubility
It is soluble in water (partly).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.Incompatible with strong bases, strong oxidizing agents.
RUO – Research Use Only
General References:
- Charles T. West.; Stephen J. Donnelly.; Dale A. Kooistra.; Michael P. Doyle. Silane reductions in acidic media. II. Reductions of aryl aldehydes and ketones by trialkylsilanes in trifluoroacetic acid. Selective method for converting the carbonyl group to methylene. J. Org. Chem. 1973, 38, (15), 2675-2681.
- C. George.; R. S. Strekowski.; J. Kleffmann.; K. Stemmler M. Ammann. Photoenhanced uptake of gaseous NO2 on solid organic compounds: a photochemical source of HONO. Faraday Discuss. 2005, 130, (15), 195-210.