| Identification | More | [Name]
ETHYL PHENYLPROPIOLATE | [CAS]
2216-94-6 | [Synonyms]
ETHYL-3-PHENYLPROPIOLATE
ETHYL PHENYLACETYLENECARBOXYLATE
ETHYL PHENYLPROPIOLATE
PHENYLACETYLENECARBOXYLIC ACID ETHYL ESTER
PHENYLPROPIOLIC ACID ETHYL ESTER
RARECHEM AL BI 0668
TIMTEC-BB SBB008827
2-Propynoic acid, 3-phenyl-, ethyl ester
3-phenyl-2-propynoicaciethylester
Ethyl 3-phenyl-2-propynoate
Ethyl 3-phenylpropynoate
Ethyl phenylpropriolate
Ethyl phenylpropynoate
ethyl3-phenyl-2-propynoate
ethyl3-phenylpropynoate
ethylphenylpropynoate
Phenylacetylene monocarboxylic acid ethyl ester
phenyl-propiolicaciethylester
Propiolic acid, phenyl-, ethyl ester
Ethyl phenylacetylenecarboxylate~Phenylpropiolic acid ethyl ester | [EINECS(EC#)]
218-703-8 | [Molecular Formula]
C11H10O2 | [MDL Number]
MFCD00009185 | [Molecular Weight]
174.2 | [MOL File]
2216-94-6.mol |
| Safety Data | Back Directory | [Risk Statements ]
R36/38:Irritating to eyes and skin . | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
UE0110000
| [HS Code ]
29163990 |
| Hazard Information | Back Directory | [General Description]
Clear pale yellow liquid. | [Reactivity Profile]
Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. | [Air & Water Reactions]
Insoluble in water. | [Fire Hazard]
This compound is combustible. | [Chemical Properties]
clear yellowish liquid | [Uses]
Ethyl phenylpropiolate, is an important organic intermediate. It is also used as an intermediate in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 50, p. 2372, 1985 DOI: 10.1021/jo00213a034
Synthesis, p. 498, 1987 DOI: 10.1055/s-1987-27983 |
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