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About This Item
Linear Formula:
C2H5C6H4CO2H
CAS Number:
Molecular Weight:
150.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
62-66 °C (lit.)
SMILES string
CCc1ccccc1C(O)=O
InChI
1S/C9H10O2/c1-2-7-5-3-4-6-8(7)9(10)11/h3-6H,2H2,1H3,(H,10,11)
InChI key
CGMMPMYKMDITEA-UHFFFAOYSA-N
Related Categories
Application
2-Ethylbenzoic acid has been employed:
- as substrate for microbial asymmetric synthesis of (S)-3-methylphthalide
- in synthesis of γ-lactones and bis(2-ethylbenzoyl)peroxide
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Cynthia D Fast et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 37(11), 3085-3101 (2017-02-12)
Fear- and stress-induced activity in the amygdala has been hypothesized to influence sensory brain regions through the influence of the amygdala on neuromodulatory centers. To directly examine this relationship, we used optical imaging to observe odor-evoked activity in populations of
Intramolecular hydrogen-atom transfer in 2-alkylbenzoyloxyl radicals as studied by transient absorption kinetics and product analyses on the photodecomposition of bis (2-alkylbenzoyl) peroxides.
Wang J, et al.
Bulletin of the Chemical Society of Japan, 68(4), 1213-1219 (1995)
Microbial asymmetric syntheses of 3-alkylphthalide derivatives.
Kitayama T.
Tetrahedron Asymmetry, 8(22), 3765-3774 (1997)
An improved method for the synthesis of ?-lactones using sodium bromate and sodium hydrogen sulfite.
Hayat S, et al.
Tetrahedron Letters, 42(9), 1647-1649 (2001)
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