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308080

Sigma-Aldrich

Benzoylnitromethane

98%

Synonym(s):

α-Nitroacetophenone

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About This Item

Linear Formula:
C6H5COCH2NO2
CAS Number:
614-21-1
Molecular Weight:
165.15
MDL number:
MFCD00010218
UNSPSC Code:
12352100
PubChem Substance ID:
24858646
NACRES:
NA.22
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Quality Level

100

Assay

98%

mp

105-107 °C (lit.)

storage temp.

2-8°C

SMILES string

[O-][N+](=O)CC(=O)c1ccccc1

InChI

1S/C8H7NO3/c10-8(6-9(11)12)7-4-2-1-3-5-7/h1-5H,6H2

InChI key

JTWHVBNYYWFXSI-UHFFFAOYSA-N

Related Categories

General description

The kinetics of proton transfer from benzoylnitromethane to various bases was studied[1].

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ5375
STBH8931
STBG8568
STBD8427V
STBC7265V

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Claude F. Bernasconi et al.
The Journal of organic chemistry, 62(23), 8162-8170 (2001-10-24)
The replacement of a hydrogen in nitromethane and in phenylnitromethane by the PhCO group has a strong acidifying effect, i.e., PhCOCH(2)NO(2), 5, is 5.8, 6.6, and 8.6 pK(a) units more acidic than CH(3)NO(2) in water, 50% DMSO-50% water (v/v), and
Parham Taslimi
Archiv der Pharmazie, 353(11), e2000210-e2000210 (2020-09-03)
In this study, the acetophenone derivatives 1-6 were found to be effective inhibitor molecules for α-glycosidase, human carbonic anhydrases I and II (hCA I/II), and acetylcholinesterase (AChE), with Ki values in the range of 167.98 ± 25.06 to 304.36 ± 65.45 µM for α-glycosidase, 555.76 ± 56.07

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