| Identification | Back Directory | [Name]
ETHYL 2 3-BUTADIENOATE 95 | [CAS]
14369-81-4 | [Synonyms]
2,3-Butadienoate
ethyl buta-2,3-dienoate
Ethyl2,3-Butadienoate>
ETHYL 2 3-BUTADIENOATE 95
ETHYL 2,3-BUTADIENOATE 95%
2,3-Butadienoic Acid Ethyl Ester | [Molecular Formula]
C6H8O2 | [MDL Number]
MFCD01863567 | [MOL File]
14369-81-4.mol | [Molecular Weight]
112.127 |
| Chemical Properties | Back Directory | [Boiling point ]
80 °C60 mm Hg(lit.)
| [density ]
0.966 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.46(lit.)
| [Fp ]
116 °F
| [storage temp. ]
<0°C | [form ]
clear liquid | [color ]
Colorless to Light yellow | [λmax]
209nm(MeOH)(lit.) |
| Safety Data | Back Directory | [Risk Statements ]
10 | [RIDADR ]
UN 1993 3/PG 2
| [WGK Germany ]
3
| [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29161900 |
| Hazard Information | Back Directory | [Uses]
Ethyl 2,3-butadienoate may be used in the synthesis of dihydropyrans by reacting with acyclic enones. It may also be used to synthesize spiranic heterocycles by reacting with heterocyclic bis-arylidene ketones via phosphine-catalyzed [3+2] annulations. | [Uses]
Ethyl Buta-2,3-dienoate is a useful reactant for the synthesis of 9H-?pyrrolo[1,?2-?a]?indole derivatives via a phosphine-?promoted Michael addn.?/intramol. Wittig reaction. | [General Description]
Ethyl 2,3-butadienoate is an α-allenic ester. The reaction of ethyl 2,3-butadienoate with N-tosylated imines in the presence of DABCO (1,4-diazabicyclo[2.2.2]octane) or DMAP (4-dimethylaminopyridine) forms azetidine derivatives or novel dihydropyridine derivatives respectively. The performance of bifunctional N-acyl aminophosphines to catalyze the asymmetric [3+2] cycloaddition of phenylidenemalononitrile with ethyl 2,3-butadienoate has been evaluated. |
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TCI Europe
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320-37350700 |
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TCI AMERICA
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800-4238616 |
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https://www.tcichemicals.com/en/us/index.html |
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