161268
4-Phenyl-3-butyn-2-one
96%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
C6H5C≡CCOCH3
CAS Number:
Molecular Weight:
144.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-327-1
MDL number:
Assay:
96%
Form:
liquid
InChI key
UPEUQDJSUFHFQP-UHFFFAOYSA-N
InChI
1S/C10H8O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-6H,1H3
SMILES string
CC(=O)C#Cc1ccccc1
assay
96%
form
liquid
refractive index
n20/D 1.574 (lit.)
bp
75-76 °C/0.8 mmHg (lit.)
density
0.99 g/mL at 25 °C (lit.)
functional group
ketone, phenyl
storage temp.
2-8°C
General description
4-Phenyl-3-butyn-2-one is an α,β-ketoalkyne. Reaction of 4-phenyl-3-butyn-2-one with bromine chloride and iodine monochloride in CH2Cl2, CH2Cl2/pyridine and MeOH are studied. Reduction of 4-phenyl-3-butyn-2-one in THF solution has been reported.
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Victor L Heasley et al.
The Journal of organic chemistry, 67(7), 2183-2187 (2002-04-02)
The reactions of 3-butyn-2-one (1), 3-hexyn-2-one (2), and 4-phenyl-3-butyn-2-one (3) with bromine chloride (BrCl) and iodine monochloride (ICl) in CH(2)Cl(2), CH(2)Cl(2)/pyridine, and MeOH are described. The data show that the major products in CH(2)Cl(2) are (Z)-AM (anti-Markovnikov) regioisomers. With the
Improved procedure for the asymmetric reduction of prochiral ketones by B-3-pinanyl-9-borabicyclo [3.3. 1] nonane.
Brown HC and Pai GG.
The Journal of Organic Chemistry, 47(8), 1606-1608 (1982)
Reductive metabolism of an alpha,beta-ketoalkyne, 4-phenyl-3-butyn-2-one, by rat liver preparations.
Shigeyuki Kitamura et al.
Drug metabolism and disposition: the biological fate of chemicals, 30(4), 414-420 (2002-03-20)
The reduction of the triple bond and carbonyl group of an alpha,beta-ketoalkyne, 4-phenyl-3-butyn-2-one (PBYO), by rat liver microsomes and cytosol was investigated. The triple-bond-reduced product trans-4-phenyl-3-buten-2-one (PBO) and the carbonyl-reduced product 4-phenyl-3-butyn-2-ol (PBYOL) were formed when PBYO was incubated with
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service