meptazinol para-aminophenylacetic acid carbamate hydrochloride

Base Information

Chemical Name:meptazinol para-aminophenylacetic acid carbamate hydrochloride
CAS No.:1314003-16-1
Molecular Formula:C₂₄H₃₀N₂O₄*ClH
Molecular Weight:446.974
Hs Code.:

Synonyms:meptazinol para-aminophenylacetic acid carbamate hydrochloride

Suppliers and Price of meptazinol para-aminophenylacetic acid carbamate hydrochloride

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

Total 0 raw suppliers

Chemical Property of meptazinol para-aminophenylacetic acid carbamate hydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of meptazinol para-aminophenylacetic acid carbamate hydrochloride

There total 3 articles about meptazinol para-aminophenylacetic acid carbamate hydrochloride 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: 46.0%

: 1314003-57-0
meptazinol 4-aminophenylacetic acid tert-butyl ester carbamate

: 1314003-16-1
meptazinol para-aminophenylacetic acid carbamate hydrochloride

Guidance literature:: meptazinol 4-aminophenylacetic acid tert-butyl ester carbamate; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 3h;

With hydrogenchloride; In tetrahydrofuran; 1,4-dioxane;

Reference yield:

: 174579-31-8
(4-aminophenyl)acetic acid tert-butyl ester

: 1314003-16-1
meptazinol para-aminophenylacetic acid carbamate hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate / dichloromethane; toluene; water / 0.5 h / 5 - 20 °C

2.1: sodium hydrogencarbonate / chloroform; water

2.2: 16 h / 50 °C

3.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

With sodium hydrogencarbonate; trifluoroacetic acid; In dichloromethane; chloroform; water; toluene; 1.1: Schotten-Baumann Reaction;

Reference yield:

: 181519-06-2
tert-butyl 2-(4-isocyanatophenyl)acetate

: 1314003-16-1
meptazinol para-aminophenylacetic acid carbamate hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydrogencarbonate / chloroform; water

1.2: 16 h / 50 °C

2.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

With sodium hydrogencarbonate; trifluoroacetic acid; In dichloromethane; chloroform; water;