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Sigma-Aldrich

1-Phenyl-2-propyn-1-one

≥95.0% (HPLC)

Synonym(s):

1-Phenylpropynone, Ethynyl phenyl ketone

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About This Item

Empirical Formula (Hill Notation):
C9H6O
CAS Number:
Molecular Weight:
130.14
Beilstein/REAXYS Number:
606216
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥95.0% (HPLC)

form

lumps

storage temp.

2-8°C

SMILES string

O=C(C#C)c1ccccc1

InChI

1S/C9H6O/c1-2-9(10)8-6-4-3-5-7-8/h1,3-7H

InChI key

JITPLZPWKYUTDM-UHFFFAOYSA-N

Related Categories

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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L Jaenicke et al.
European journal of biochemistry, 138(2), 319-325 (1984-01-16)
3-Oxo-3-phenylpropyne and 3-oxo-3-phenylpropene were synthesized as active-site-directed irreversible inhibitors of the bitter almond hydroxynitrile lyase (EC 4.1.2.10), an FAD-protein. The substrate and competitors (e.g. benzoate) decrease the rate of the inhibitor-mediated deactivation of the enzyme. By excess addition of either
Unsaturated lactones; researches on acetylenic compounds; a new route to growth-inhibitory alpha beta-ethylenic gamma- and delta-lactones.
L J HAYNES et al.
Journal of the Chemical Society, 954-957 (1946-10-01)

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