Methyl (E)-3-pentenoate
Methyl (E)-3-pentenoate Basic information
- Product Name:
- Methyl (E)-3-pentenoate
- Synonyms:
-
- (E)-CH3CH=CHCH2C(O)OCH3
- METHYL 3-PENTENOATE
- methyl (e)-3-pentenoate
- METHYL TRANS-3-PENTENOATE
- METHYL TRANS-PENTENOIC ACID
- 3-PENTENOIC ACID METHYL ESTER
- METHYL (E)-PENT-3-ENOATE
- METHYL TRANS-3-PENTENOAT
- CAS:
- 20515-19-9
- MF:
- C6H10O2
- MW:
- 114.14
- EINECS:
- 628-216-6
- Product Categories:
-
- C6 to C7
- Carbonyl Compounds
- Esters
- Building Blocks
- C6 to C7
- Carbonyl Compounds
- Chemical Synthesis
- Organic Building Blocks
- Mol File:
- 20515-19-9.mol
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Methyl (E)-3-pentenoate Chemical Properties
- Melting point:
- 37.22°C (estimate)
- Boiling point:
- 55-56 °C/20 mmHg (lit.)
- Density
- 0.93 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.421(lit.)
- Flash point:
- 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)
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MSDS
- Language:English Provider:SigmaAldrich
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Methyl (E)-3-pentenoate Usage And Synthesis
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.
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