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M26607

Sigma-Aldrich

3′-Methylacetophenone

98%

Synonym(s):

Methyl m-tolyl ketone

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About This Item

Linear Formula:
CH3C6H4COCH3
CAS Number:
585-74-0
Molecular Weight:
134.18
Beilstein:
956637
EC Number:
209-561-8
MDL number:
MFCD00008742
UNSPSC Code:
12352100
PubChem Substance ID:
24896754
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.529 (lit.)

bp

218-220 °C (lit.)

mp

−9 °C (lit.)

density

0.986 g/mL at 25 °C (lit.)

SMILES string

CC(=O)c1cccc(C)c1

InChI

1S/C9H10O/c1-7-4-3-5-9(6-7)8(2)10/h3-6H,1-2H3

InChI key

FSPSELPMWGWDRY-UHFFFAOYSA-N

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

185.0 °F - closed cup

Flash Point(C)

85 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Manuela Panić et al.
Biotechnology letters, 41(2), 253-262 (2018-12-05)
Chiral building blocks [(S)-1-(3-methylphenyl)ethanol, (S)-1-(3,4-dimethylphenyl)ethanol and (S)-1-(2,4,6-trimethylphenyl)ethanol] for drug synthesis were prepared using two green approaches: (1) the yeast Saccharomyces cerevisiae as the biocatalyst and (2) the natural deep eutectic solvents (NADES) as the alternative solvents. Three different NADES with
Huiying Song et al.
Journal of chromatography. A, 1532, 124-135 (2017-12-10)
The accuracy of the longitudinal diffusion term (b-term) plays a vital role in the study of mass transfer mechanisms in high performance liquid chromatography (HPLC). In this study, three commonly used methodologies (peak parking; fitting of an experimental van Deemter
Kunpeng Li et al.
Scientific reports, 7(1), 3081-3081 (2017-06-10)
(S)-carbonyl reductase II (SCRII) from Candida parapsilosis is a short-chain alcohol dehydrogenase/reductase. It catalyses the conversion of 2-hydroxyacetophenone to (S)-1-phenyl-1,2-ethanediol with low efficiency. Sortase was reported as a molecular "stapler" for site-specific protein conjugation to strengthen or add protein functionality.

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