3-Vinylphenyl ethyl(methyl)-carbamate

Base Information

Chemical Name:3-Vinylphenyl ethyl(methyl)-carbamate
CAS No.:1346602-84-3
Molecular Formula:C₁₂H₁₅NO₂
Molecular Weight:205.257
Hs Code.:
Mol file:1346602-84-3.mol

Synonyms:RA03;Y7449;N-Ethyl-N-methyl-3-ethenylphenyl Carbamate;3-vinylphenyl ethyl(methyl)carbamate;3-vinylphenyl N-ethyl-N-methylcarbamate;N-Ethyl-N-methyl-3-vinylphenyl Carbamate;

Suppliers and Price of 3-Vinylphenyl ethyl(methyl)-carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
N-Ethyl-N-methyl-3-vinylphenylCarbamate
250mg
$ 1455.00

Medical Isotopes, Inc.
N-Ethyl-N-methyl-3-vinylphenylCarbamate
25 mg
$ 650.00

Crysdot
3-Vinylphenylethyl(methyl)carbamate 95%
250mg
$ 235.00

Alichem
3-Vinylphenylethyl(methyl)carbamate
5g
$ 1035.86

aablocks
3-Vinylphenylethyl(methyl)carbamate
250mg
$ 1470.00

aablocks
3-Vinylphenylethyl(methyl)carbamate
25mg
$ 315.00

Total 12 raw suppliers

Chemical Property of 3-Vinylphenyl ethyl(methyl)-carbamate

Chemical Property:

Boiling Point:303.5±25.0 °C(Predicted)
PKA:-1.47±0.70(Predicted)
PSA：29.54000
Density:1.061±0.06 g/cm3(Predicted)
LogP:2.78010
Storage Temp.:2-8°C

Purity/Quality:

99% ^*data from raw suppliers

N-Ethyl-N-methyl-3-vinylphenylCarbamate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses A related compound of Rivastigmine (R541000), a cholinesterase inhibitor. Rivastigmine USP Related Compound F.

Technology Process of 3-Vinylphenyl ethyl(methyl)-carbamate

There total 4 articles about 3-Vinylphenyl ethyl(methyl)-carbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: C₁₉H₂₃NO₅S

: 1346602-84-3
3-vinylphenyl N-ethyl-N-methylcarbamate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; at 140 ℃; for 3h;
DOI:10.14233/ajchem.2013.13473

Reference yield:

: 855300-09-3
1-(N-ethyl-N-methylaminocarbonyloxy)-3-acetylbenzene

: 1346602-84-3
3-vinylphenyl N-ethyl-N-methylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetrahydroborate / ethanol / 1 h / 0 - 20 °C

2: pyridine / 0 - 20 °C

3: 1,8-diazabicyclo[5.4.0]undec-7-ene / 3 h / 140 °C

With pyridine; sodium tetrahydroborate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol;
DOI:10.14233/ajchem.2013.13473

Reference yield:

: 121-71-1
3-Hydroxyacetophenone

: 1346602-84-3
3-vinylphenyl N-ethyl-N-methylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / acetone / 3 h / Reflux

2: sodium tetrahydroborate / ethanol / 1 h / 0 - 20 °C

3: pyridine / 0 - 20 °C

4: 1,8-diazabicyclo[5.4.0]undec-7-ene / 3 h / 140 °C

With pyridine; sodium tetrahydroborate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; acetone;
DOI:10.14233/ajchem.2013.13473