Basic information Safety Supplier Related

Methyl (E)-3-pentenoate

Basic information Safety Supplier Related

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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Safety Information

Risk Statements 
10-22
Safety Statements 
16
RIDADR 
UN 3272 3/PG 3
WGK Germany 
3
10
HS Code 
2916.19.3000
HazardClass 
3.2
PackingGroup 
III

MSDS

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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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