| Weight | 121.115 g/mol |
|---|---|
| Formula | C7H5O2- |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
benzoate (65-85-0, 766-76-7)
Benzoates · Benzoic Acids
Score:
#235 in Physics
,
#663 in Biology
,
#710 in Chemistry
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- An Extended Table of Hammett Substitutent Constants Based on the Ionization of Substituted Benzoic Acids (Journal of Organic Chemistry, 1958)
- Resolution by high-performance liquid chromatography using polysaccharide carbamates and benzoates as chiral stationary phases (Journal of Chromatography A, 1994)
- Some alkyl hydroxy benzoate preservatives (parabens) are estrogenic. (Toxicology and Applied Pharmacology, 1998)
- An Efficient WasteFree Oxidative Coupling via Regioselective CH Bond Cleavage: Rh/CuCatalyzed Reaction of Benzoic Acids with Alkynes and Acrylates under Air. (ChemInform, 2007)
- Crystal engineering approach to forming cocrystals of amine hydrochlorides with organic acids. Molecular complexes of fluoxetine hydrochloride with benzoic, succinic, and fumaric acids (Journal of the American Chemical Society, 2004)
- Polar and Steric Substituent Constants for Aliphatic and o-Benzoate Groups from Rates of Esterification and Hydrolysis of Esters1 (Journal of the American Chemical Society, 1952)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Benzoates
- Benzoic Acids
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SMILESC1=CC=C(C=C1)C(=O)[O-]
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InChIKeyWPYMKLBDIGXBTP-UHFFFAOYSA-M
- Pubchem - benzoate
- Wikipedia - benzoate
Benzoic acid , C7H6O2 (or C6H5COOH), is a colorless crystalline solid and a simple aromatic carboxylic acid. The name is derived from gum benzoin, which was for a long time its only known source. Benzoic acid occurs naturally in many plants and serves as an intermediate in the biosynthesis of many secondary metabolites.
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