C₂₂H₃₄N₄O₅S

Base Information

Chemical Name:C₂₂H₃₄N₄O₅S
CAS No.:99701-49-2
Molecular Formula:C₂₂H₃₄N₄O₅S
Molecular Weight:466.602
Hs Code.:

C<sub>22</sub>H<sub>34</sub>N<sub>4</sub>O<sub>5</sub>S

Synonyms:

Suppliers and Price of C₂₂H₃₄N₄O₅S

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 C₂₂H₃₄N₄O₅S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₂H₃₄N₄O₅S

There total 3 articles about C₂₂H₃₄N₄O₅S 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:

: 77543-00-1,65929-03-5
N-formylmethionylleucylphenylalanine methyl ester

: 99701-49-2
C₂₂H₃₄N₄O₅S

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide) / tetrahydrofuran / 1 h / 0 °C

2: 60 percent / triethylamine, mercuric acetate, hydroxylamine hydrochloride / acetonitrile

With thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide); hydroxylamine hydrochloride; mercury(II) diacetate; triethylamine; In tetrahydrofuran; acetonitrile;
DOI:10.1139/v85-511

Reference yield:

: 77542-78-0
Boc-Met-Leu-Phe-OMe

: 99701-49-2
C₂₂H₃₄N₄O₅S

Guidance literature:: Multi-step reaction with 4 steps

1: 98percent formic acid / 3 h / Ambient temperature

2: EEDQ / CHCl₃ / 8 h / Ambient temperature

3: 70 percent / thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide) / tetrahydrofuran / 1 h / 0 °C

4: 60 percent / triethylamine, mercuric acetate, hydroxylamine hydrochloride / acetonitrile

With formic acid; thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide); hydroxylamine hydrochloride; mercury(II) diacetate; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; triethylamine; In tetrahydrofuran; chloroform; acetonitrile;
DOI:10.1139/v85-511

Reference yield:

: 77542-94-0
H-Met-Leu-Phe-OMe formate salt

: 99701-49-2
C₂₂H₃₄N₄O₅S

Guidance literature:: Multi-step reaction with 3 steps

1: EEDQ / CHCl₃ / 8 h / Ambient temperature

2: 70 percent / thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide) / tetrahydrofuran / 1 h / 0 °C

3: 60 percent / triethylamine, mercuric acetate, hydroxylamine hydrochloride / acetonitrile

With thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide); hydroxylamine hydrochloride; mercury(II) diacetate; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; triethylamine; In tetrahydrofuran; chloroform; acetonitrile;
DOI:10.1139/v85-511