ethyl 1-ethoxycarbonylMethylindole-2-carboxylate

Base Information

Chemical Name:ethyl 1-ethoxycarbonylMethylindole-2-carboxylate
CAS No.:256931-80-3
Molecular Formula:C15H17NO4
Molecular Weight:275.29978
Hs Code.:2933790090
Mol file:256931-80-3.mol

Synonyms:ethyl 1-ethoxycarbonylMethylindole-2-carboxylate;Ethyl 1-(2-ethoxy-2-oxoethyl)-1H-indole-2-carboxylate

Suppliers and Price of ethyl 1-ethoxycarbonylMethylindole-2-carboxylate

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

Crysdot
Ethyl1-(2-ethoxy-2-oxoethyl)-1H-indole-2-carboxylate 95+%
1g
$ 374.00

Chemenu
ethyl1-(2-ethoxy-2-oxoethyl)-1H-indole-2-carboxylate 95%
1g
$ 354.00

Alichem
Ethyl1-(2-ethoxy-2-oxoethyl)-1H-indole-2-carboxylate
1g
$ 400.00

Total 6 raw suppliers

Chemical Property of ethyl 1-ethoxycarbonylMethylindole-2-carboxylate

Chemical Property:

PSA：57.53000
LogP:2.38110
Storage Temp.:2-8°C

Purity/Quality:

98% ^*data from raw suppliers

Ethyl1-(2-ethoxy-2-oxoethyl)-1H-indole-2-carboxylate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of ethyl 1-ethoxycarbonylMethylindole-2-carboxylate

There total 2 articles about ethyl 1-ethoxycarbonylMethylindole-2-carboxylate 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: 98.8%

: 3770-50-1,117770-52-2
2-carbethoxyindole

: 105-36-2
ethyl bromoacetate

: 256931-80-3
ethyl 1-(2-ethoxy-2-oxoethyl)-1H-indole-2-carboxylate

Guidance literature:: With potassium carbonate; In acetonitrile; at 80 ℃; for 20h;

Reference yield:

: 600-22-6
pyruvic acid methyl ester

: 256931-80-3
ethyl 1-(2-ethoxy-2-oxoethyl)-1H-indole-2-carboxylate

Guidance literature:: With hydrogenchloride;
DOI:10.1139/v52-049

Reference yield: 78.0%

: 256931-80-3
ethyl 1-(2-ethoxy-2-oxoethyl)-1H-indole-2-carboxylate

: 4559-70-0
Diphenylphosphine oxide

: 1620064-62-1
C₂₇H₂₆NO₅P

Guidance literature:: With triphenylphosphine; copper(l) chloride; In acetonitrile; at 50 ℃; for 24h; stereoselective reaction; Inert atmosphere;
DOI:10.1039/c4cc01815j