ChemicalBook--->CAS DataBase List--->14369-81-4

14369-81-4

14369-81-4 Structure

14369-81-4 Structure
IdentificationBack 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 PropertiesBack 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.)
[InChI]

1S/C6H8O2/c1-3-5-6(7)8-4-2/h5H,1,4H2,2H3
[InChIKey]

GLSUOACRAMLJIW-UHFFFAOYSA-N
[SMILES]

[H]C([H])=C=C([H])C(=O)OCC
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)
GHS02
[Signal word ]

Warning
[Hazard statements ]

H226
[Precautionary statements ]

P210-P233-P240-P241-P242-P243
[Risk Statements ]

10
[RIDADR ]

UN 1993 3/PG 2
[WGK Germany ]

3
[HazardClass ]

3
[PackingGroup ]

III
[HS Code ]

29161900
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Flam. Liq. 3
Hazard InformationBack 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.
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 2 3-BUTADIENOATE 95(14369-81-4)1HNMR
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