Skip to Content
Merck
CN

362379

Methyl trans-3-methoxyacrylate

97%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CH3OCH=CHCO2CH3
CAS Number:
Molecular Weight:
116.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
412-900-4
MDL number:
Assay:
97%
Form:
liquid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

AUTCCPQKLPMHDN-ONEGZZNKSA-N

InChI

1S/C5H8O3/c1-7-4-3-5(6)8-2/h3-4H,1-2H3/b4-3+

SMILES string

CO\C=C\C(=O)OC

assay

97%

form

liquid

refractive index

n20/D 1.451 (lit.)

bp

56 °C/18 mmHg (lit.)

density

1.08 g/mL at 25 °C (lit.)

functional group

ester, ether

storage temp.

2-8°C

Quality Level

Application

Methyl trans-3-methoxyacrylate may be used in the preparation of:
  • 5- hydroxyquinolines
  • 7-hydroxyquinolines
  • methyl 5-methoxyquinoline-3-carboxylate

pictograms

Exclamation mark

signalword

Warning

hcodes

pcodes

Hazard Classifications

Skin Sens. 1

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

145.4 °F - closed cup

flash_point_c

63 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Pierre Bohn et al.
Organic & biomolecular chemistry, 7(12), 2612-2618 (2009-06-09)
This work deals with the design of a bio-oxidisable prodrug strategy for the development of new central selective acetylcholinesterase inhibitors. This prodrug approach is expected to reduce peripheral anticholinesterase activity responsible for various side effects observed with presently marketed AChE

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service