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Merck

137235

Sigma-Aldrich

3′,4′-Dimethylacetophenone

98%

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50 ML
US$190.00
5 X 50 ML
US$745.00

US$190.00


Estimated to ship on29 March 2025


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50 ML
US$190.00
5 X 50 ML
US$745.00

About This Item

Linear Formula:
(CH3)2C6H3COCH3
CAS Number:
Molecular Weight:
148.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

form:
liquid
Assay:
98%

US$190.00


Estimated to ship on29 March 2025


Request a Bulk Order

Quality Level

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

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This Item
H7033S2404S7899
form

liquid (2x concentrate)

form

solution

form

liquid

form

liquid

storage temp.

−20°C

storage temp.

room temp

storage temp.

2-8°C

storage temp.

room temp

foreign activity

DNAses, RNases, NICKases, endonucleases, and exonucleases, none detected

foreign activity

-

foreign activity

-

foreign activity

-

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[1].

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

217.4 °F - closed cup

Flash Point(C)

103.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), 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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