seryl-tetrahydroisoquinolinecarbonyl-octahydroindole-2-carbonyl-arginine

Base Information

Chemical Name:seryl-tetrahydroisoquinolinecarbonyl-octahydroindole-2-carbonyl-arginine
CAS No.:148416-85-7
Molecular Formula:C₂₈H₄₁N₇O₆
Molecular Weight:571.677
Hs Code.:
Mol file:148416-85-7.mol

Synonyms:seryl-tetrahydroisoquinolinecarbonyl-octahydroindole-2-carbonyl-arginine

Suppliers and Price of seryl-tetrahydroisoquinolinecarbonyl-octahydroindole-2-carbonyl-arginine

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 2 raw suppliers

Chemical Property of seryl-tetrahydroisoquinolinecarbonyl-octahydroindole-2-carbonyl-arginine

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.53g/cm³

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of seryl-tetrahydroisoquinolinecarbonyl-octahydroindole-2-carbonyl-arginine

There total 1 articles about seryl-tetrahydroisoquinolinecarbonyl-octahydroindole-2-carbonyl-arginine 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:

: 78879-20-6,144069-68-1,115962-35-1
D-N-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinolinoline-3-carboxylic acid

: 78545-07-0
(S)-3-(benzoyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acid

: 186096-30-0
Boc-L-octahydroindole-2S-carboxylic acid

: 148416-85-7
H-Ser-D-Tic-Oic-Arg-OH

Guidance literature:: With hydrogen fluoride; methoxybenzene; trifluoroacetic acid; diisopropyl-carbodiimide; Multistep reaction;
DOI:10.1021/jm00062a018