137235
3′,4′-Dimethylacetophenone
98%
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About This Item
Fórmula lineal:
(CH3)2C6H3COCH3
Número de CAS:
Peso molecular:
148.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
98%
form
liquid
refractive index
n20/D 1.538 (lit.)
bp
243 °C (lit.)
density
1.001 g/mL at 25 °C (lit.)
functional group
ketone
SMILES string
CC(=O)c1ccc(C)c(C)c1
InChI
1S/C10H12O/c1-7-4-5-10(9(3)11)6-8(7)2/h4-6H,1-3H3
InChI key
WPRAXAOJIODQJR-UHFFFAOYSA-N
Application
3′,4′-Dimethylacetophenone was used as starting reagent in the synthesis of 4-[5-(3,4-dimethylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenecarboxyamide.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
217.4 °F - closed cup
flash_point_c
103.00 °C - closed cup
ppe
Eyeshields, Gloves
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Jiuxiang Zhu et al.
Journal of the National Cancer Institute, 94(23), 1745-1757 (2002-12-05)
The cyclooxygenase-2 (COX-2) inhibitor celecoxib is thought to act as a chemopreventive agent by sensitizing cancer cells to apoptotic signals. Other COX-2 inhibitors, such as rofecoxib, are two orders of magnitude less potent than celecoxib at inducing apoptosis. The molecular
Shakila K Evans et al.
Chemical biology & drug design, 75(3), 333-337 (2010-07-28)
Acetophenones were screened for activity against positive phototaxis of Chlamydomonas cells, a process that requires co-ordinated flagellar motility. The structure-activity relationships of a series of acetophenones are reported, including acetophenones that affect flagellar motility and cell viability. Notably, 4-methoxyacetophenone, 3,4-dimethoxyacetophenone
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