6-bromo-8-(3-tert-butoxycarbonylamino-1-propynyl)-2-(4-diethylaminophenyl)-3-isobutyroxychromone

Base Information

Chemical Name:6-bromo-8-(3-tert-butoxycarbonylamino-1-propynyl)-2-(4-diethylaminophenyl)-3-isobutyroxychromone
CAS No.:1192742-70-3
Molecular Formula:C₃₁H₃₅BrN₂O₆
Molecular Weight:611.533
Hs Code.:

Synonyms:6-bromo-8-(3-tert-butoxycarbonylamino-1-propynyl)-2-(4-diethylaminophenyl)-3-isobutyroxychromone

Suppliers and Price of 6-bromo-8-(3-tert-butoxycarbonylamino-1-propynyl)-2-(4-diethylaminophenyl)-3-isobutyroxychromone

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 6-bromo-8-(3-tert-butoxycarbonylamino-1-propynyl)-2-(4-diethylaminophenyl)-3-isobutyroxychromone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-bromo-8-(3-tert-butoxycarbonylamino-1-propynyl)-2-(4-diethylaminophenyl)-3-isobutyroxychromone

There total 1 articles about 6-bromo-8-(3-tert-butoxycarbonylamino-1-propynyl)-2-(4-diethylaminophenyl)-3-isobutyroxychromone 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: 16.0%

: 1192742-69-0
6,8-dibromo-2-(4-diethylaminophenyl)-3-isobutyroxychromone

: 92136-39-5
N-tert-Butoxycarbonyl-1-amino-3-propyne

: 1192742-70-3
6-bromo-8-(3-tert-butoxycarbonylamino-1-propynyl)-2-(4-diethylaminophenyl)-3-isobutyroxychromone

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In tetrahydrofuran; at 120 ℃; for 0.5h; Microwave irradiation; Inert atmosphere;
DOI:10.1002/chem.200900279