di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide

Base Information

Chemical Name:di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide
CAS No.:1350442-00-0
Molecular Formula:C₂₄H₃₄N₄O₆S
Molecular Weight:506.623
Hs Code.:

Synonyms:di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide

Suppliers and Price of di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide

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 di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide

There total 2 articles about di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide 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:

: 1350440-49-1
di-(3-(N-t-butoxycarbonyl-N-methylamino)-4-nitrophenyl) sulfide

: 1350442-00-0
di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; at 20 ℃; for 72h;

Reference yield:

: 299176-17-3
N-(2-nitro-5-chlorophenyl)-N-methylcarbamic acid t-butyl ester

: 1350442-00-0
di-(4-hydroxyamino-3-(N-t-butoxycarbonyl-N-methylamino)phenyl) sulfide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium thioacetate / N,N-dimethyl-formamide / 8.5 h / 180 °C

2: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 72 h / 20 °C

With palladium 10% on activated carbon; hydrogen; potassium thioacetate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;