543195
Methyl phenylpropiolate
97%
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About This Item
Linear Formula:
C6H5C≡CCO2CH3
CAS Number:
Molecular Weight:
160.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
Methyl phenylpropiolate, 97%
InChI key
JFGWPXKGINUNDH-UHFFFAOYSA-N
SMILES string
COC(=O)C#Cc1ccccc1
InChI
1S/C10H8O2/c1-12-10(11)8-7-9-5-3-2-4-6-9/h2-6H,1H3
assay
97%
refractive index
n20/D 1.5590 (lit.)
bp
109-112 °C/2 mmHg (lit.)
density
1.086 g/mL at 25 °C (lit.)
functional group
ester
phenyl
Quality Level
Related Categories
Application
Methyl phenylpropiolate may be used in the synthesis of:
- bicyclohexadienes
- cis-methyl cinnamate
- (E)-alkyl 3-(dialkoxyphosphoryl)-3-phenylacrylate derivatives
General description
Organoiron carbonyl complexes are obtained by reacting methyl phenylpropiolate with Fe2(CO)9.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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P Andrew Evans et al.
Journal of the American Chemical Society, 127(36), 12466-12467 (2005-09-08)
Transition metal-catalyzed [m+n+o] carbocyclization reactions provide powerful methods for the construction of complex polycyclic systems that are generally not accessible through classical pericyclic reactions. We have developed the first regio- and enantioselective crossed intermolecular rhodium-catalyzed [2+2+2] carbocyclization of carbon- and
Preparation and Structures of Methyl Phenylpropiolate-Iron Carbonyl Complexes. A New Dicarbonyl-p-cyclopentadienyloxy-s-vinyliron Compound.
Dahl LF, et al.
Journal of the American Chemical Society, 88(3), 446-452 (1966)
Steric effects on reactivity in silicon chemistry.
Cartledge FK.
Organometallics, 2(3), 425-430 (1983)
The catalyst-free addition of dialkyl phosphites on the triple bond of alkyl phenylpropiolates under microwave conditions.
Balint E, et al.
Current Catalysis, 4(1), 57-64 (2015)
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