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20515-19-9

20515-19-9 Structure

20515-19-9 Structure
IdentificationMore
[Name]

Methyl (E)-3-pentenoate
[CAS]

20515-19-9
[Synonyms]

3-PENTENOIC ACID METHYL ESTER
METHYL 3-PENTENOATE
methyl (e)-3-pentenoate
METHYL TRANS-3-PENTENOATE
METHYL TRANS-PENTENOIC ACID
(E)-CH3CH=CHCH2C(O)OCH3
METHYL (E)-PENT-3-ENOATE
[EINECS(EC#)]

212-453-3
[Molecular Formula]

C6H10O2
[MDL Number]

MFCD00191576
[Molecular Weight]

114.14
[MOL File]

20515-19-9.mol
Chemical PropertiesBack Directory
[Melting point ]

37.22°C (estimate)
[Boiling point ]

55-56 °C/20 mmHg (lit.)
[density ]

0.931 g/mL at 20 °C(lit.)
[refractive index ]

n20/D 1.421(lit.)
[Fp ]

75 °F
[form ]

clear liquid
[color ]

Colorless to Light yellow
[CAS DataBase Reference]

20515-19-9(CAS DataBase Reference)
[NIST Chemistry Reference]

(E)-Pent-3-enoic acid methyl ester(20515-19-9)
Safety DataBack Directory
[Risk Statements ]

R10:Flammable.
R22:Harmful if swallowed.
[Safety Statements ]

S16:Keep away from sources of ignition-No smoking .
[RIDADR ]

UN 3272 3/PG 3
[WGK Germany ]

3
[F ]

10
[HS Code ]

2916.19.3000
[HazardClass ]

3.2
[PackingGroup ]

III
Hazard InformationBack Directory
[Uses]

Methyl trans-3-pentenoate may be used for the total synthesis of phytochemicals (-)-grandinolide and (-)-sapranthin.
[General Description]

Methyl trans-3-pentenoate is an ester. Ring-closing metathesis (RCM) of methyl trans-3-pentenoate using silica- and monolith supported Grubbs-Herrmann-type catalysts has been reported. The 1,3-dipolar cycloaddition of with C-ethoxycarbonyl nitrone to form isoxazolidines has been studied.
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl (E)-3-pentenoate(20515-19-9)Raman
Methyl (E)-3-pentenoate(20515-19-9)IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

20515-19-9(sigmaaldrich)
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