Methyl pent-3-enoate

Names

[ CAS No. ]:
20515-19-9

[ Name ]:
Methyl pent-3-enoate

[Synonym ]:
methyl-3-pentenoate
3-Pentatenoic Acid Methyl Ester
Methyl trans-3-Pentenoate
Methyl (3E)-3-pentenoate
Methyl (3E)-pent-3-enoate
(E)-Pent-3-enoic acid methyl ester
3-Pentensaeuremethylester
methyl cis/trans-pent-3-enoate
EINECS 212-453-3
3-Pentenoic acid, methyl ester, (3E)-
METHYL TRANS-PENTENOIC ACID
pent-3-enoic acid methyl ester
3-Pentenoic acid, methyl ester
3-pentenoic methyl ester
Methyl pent-3-enoate
methyl 3-trans-pentenoate
MFCD00191576
3-Pentenoioc acid methyl ester

Biological Activity

[Description]:

Methyl trans-3-Pentenoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
120.8±9.0 °C at 760 mmHg

[ Molecular Formula ]:
C₆H₁₀O₂

[ Molecular Weight ]:
114.142

[ Flash Point ]:
45.9±17.1 °C

[ Exact Mass ]:
114.068077

[ PSA ]:
26.30000

[ LogP ]:
1.53

[ Vapour Pressure ]:
15.0±0.2 mmHg at 25°C

[ Index of Refraction ]:
1.422

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H226

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Risk Phrases ]:
R10

[ Safety Phrases ]:
S16

[ RIDADR ]:
UN 3272 3/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
3.2

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

Total Syntheses of (-)-Grandinolide and (-)-Sapranthin by the Sharpless Asymmetric Dihydroxylation of Methyl trans-3-Pentenoate: Elucidation of the Stereostructure of (-)-Sapranthin. Harcken C, et al.

Chemistry 4(11) , 2342-52, (1998)

Monolith-and Silica-Supported Carboxylate-Based Grubbs-Herrmann-Type Metathesis Catalysts. Krause JO, et al.

Adv. Synth. Catal. 345(8) , 996-1004, (2003)

C-Alkoxycarbonyl nitrones: building blocks for the synthesis of butenolides, lactams and modified nucleosides. Romeo G, et al.

Mini Rev. Org. Chem. 2(1) , 59-77, (2005)