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About This Item
Linear Formula:
C2H5C6H4CO2H
CAS Number:
Molecular Weight:
150.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
62-66 °C (lit.)
functional group
carboxylic acid
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
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 253804-5G | 04061831819335 |
