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Merck
CN

I18202

2-Isonitrosoacetophenone

97%

Synonym(s):

ω-(Hydroxyimino)acetophenone, ω-Isonitrosoacetophenone, Phenylglyoxaldoxime

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About This Item

Linear Formula:
C6H5COCH=NOH
CAS Number:
Molecular Weight:
149.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-539-5
Beilstein/REAXYS Number:
2041691
MDL number:
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Product Name

2-Isonitrosoacetophenone, 97%

InChI key

MLNKXLRYCLKJSS-RMKNXTFCSA-N

InChI

1S/C8H7NO2/c10-8(6-9-11)7-4-2-1-3-5-7/h1-6,11H/b9-6+

SMILES string

O\N=C\C(=O)c1ccccc1

assay

97%

mp

126-128 °C (lit.)

storage temp.

2-8°C

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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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C Meredith et al.
Journal of neurochemistry, 51(4), 1097-1101 (1988-10-01)
Phenyl di-n-pentylphosphinate is a reasonably stable easily synthesized inhibitor of neuropathy target esterase (NTE) with low anticholinesterase activity. Like phenylmethylsulphonyl fluoride it protects hens against neuropathic effects of compounds such as diisopropylphosphorofluoridate. At intervals up to 15 days after dosing
I A Dubery et al.
Phytochemistry, 50(6), 983-989 (1999-07-01)
The time- and dose-dependent occurrence of 4-(3-methyl-2-butenoxy)isonitrosoacetophenone, a gamma-irradiation-induced stress metabolite was investigated. The chemical synthesis of the compound is reported. The compound exhibits antifungal activity, as well as antioxidant activity, as indicated by its ability to scavenge reactive oxygen
Ntakadzeni E Madala et al.
Biotechnology letters, 34(7), 1351-1356 (2012-03-30)
Nicotiana tabacum cell suspensions, 2 g wet wt/ml, rapidly took up 1 mM isonitrosoacetophenone (INAP), a plant-derived stress metabolite with anti-oxidative and anti-fungal properties, producing 4'-hexopyranosyloxy-3'-methoxyisonitrosoacetophenone in 54 % yield over 18 h. Unconverted INAP was at 33 μM. UPLC-MS/MS

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