Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

(3S,6S,9S,12R,13R)-6-[1-(benzyloxy)ethyl]-3-[ (benzyloxy)methyl]-13-[(2S,3R)-3-(methoxymethoxy)hexadecan-2-yl]-12-methyl-9-(propan-2-yl)-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone

Base Information
  • Chemical Name:(3S,6S,9S,12R,13R)-6-[1-(benzyloxy)ethyl]-3-[ (benzyloxy)methyl]-13-[(2S,3R)-3-(methoxymethoxy)hexadecan-2-yl]-12-methyl-9-(propan-2-yl)-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone
  • CAS No.:1613724-91-6
  • Molecular Formula:C48H75N3O9
  • Molecular Weight:838.138
  • Hs Code.:
(3S,6S,9S,12R,13R)-6-[1-(benzyloxy)ethyl]-3-[ (benzyloxy)methyl]-13-[(2S,3R)-3-(methoxymethoxy)hexadecan-2-yl]-12-methyl-9-(propan-2-yl)-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone

Synonyms:

Suppliers and Price of (3S,6S,9S,12R,13R)-6-[1-(benzyloxy)ethyl]-3-[ (benzyloxy)methyl]-13-[(2S,3R)-3-(methoxymethoxy)hexadecan-2-yl]-12-methyl-9-(propan-2-yl)-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone
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 (3S,6S,9S,12R,13R)-6-[1-(benzyloxy)ethyl]-3-[ (benzyloxy)methyl]-13-[(2S,3R)-3-(methoxymethoxy)hexadecan-2-yl]-12-methyl-9-(propan-2-yl)-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (3S,6S,9S,12R,13R)-6-[1-(benzyloxy)ethyl]-3-[ (benzyloxy)methyl]-13-[(2S,3R)-3-(methoxymethoxy)hexadecan-2-yl]-12-methyl-9-(propan-2-yl)-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone

There total 18 articles about (3S,6S,9S,12R,13R)-6-[1-(benzyloxy)ethyl]-3-[ (benzyloxy)methyl]-13-[(2S,3R)-3-(methoxymethoxy)hexadecan-2-yl]-12-methyl-9-(propan-2-yl)-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone 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:
Guidance literature:
Multi-step reaction with 7 steps
1.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -10 °C / Inert atmosphere
2.1: dimethylsulfide borane complex / tetrahydrofuran / 4.25 h / -10 - 0 °C / Inert atmosphere
3.1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane / 2 h / 0 °C / Inert atmosphere
4.1: 2-methyl-but-2-ene; sodium dihydrogenphosphate dihydrate; sodium chlorite / water; acetonitrile / 0.33 h / 20 °C / Inert atmosphere
5.1: trifluoroacetic acid / dichloromethane / 1 h / 0 °C / Inert atmosphere
5.2: 4 h / 0 - 20 °C / Inert atmosphere
6.1: morpholine; tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran / 3 h / 25 °C / Inert atmosphere
7.1: dmap; triethylamine; 2,4,6-trichlorobenzoyl chloride / toluene / 1.67 h / 0 - 20 °C / Inert atmosphere
With morpholine; dmap; sodium chlorite; tetrakis(triphenylphosphine) palladium(0); sodium dihydrogenphosphate dihydrate; 2-methyl-but-2-ene; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; dimethylsulfide borane complex; 2,4,6-trichlorobenzoyl chloride; diisobutylaluminium hydride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; toluene; acetonitrile;
DOI:10.1002/hlca.201300255
Guidance literature:
Multi-step reaction with 15 steps
1.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.75 h / -78 °C / Inert atmosphere
1.2: -78 - -50 °C / Inert atmosphere
2.1: benzene / Reflux; Inert atmosphere
3.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -10 °C / Inert atmosphere
4.1: titanium(IV) isopropylate; diethyl (2S,3S)-tartrate; tert.-butylhydroperoxide / dichloromethane; toluene / 2.83 h / -25 °C / Molecular sieve; Inert atmosphere
5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / -45 °C / Molecular sieve; Inert atmosphere
6.1: hydrogenchloride / water; tetrahydrofuran / 0.5 h / 0 - 20 °C / Inert atmosphere
7.1: benzene / 12 h / Reflux; Inert atmosphere
8.1: N-ethyl-N,N-diisopropylamine; dmap / dichloromethane / 0.25 h / 0 °C / Inert atmosphere
8.2: 12 h / Inert atmosphere
9.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -10 °C / Inert atmosphere
10.1: dimethylsulfide borane complex / tetrahydrofuran / 4.25 h / -10 - 0 °C / Inert atmosphere
11.1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane / 2 h / 0 °C / Inert atmosphere
12.1: 2-methyl-but-2-ene; sodium dihydrogenphosphate dihydrate; sodium chlorite / water; acetonitrile / 0.33 h / 20 °C / Inert atmosphere
13.1: trifluoroacetic acid / dichloromethane / 1 h / 0 °C / Inert atmosphere
13.2: 4 h / 0 - 20 °C / Inert atmosphere
14.1: morpholine; tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran / 3 h / 25 °C / Inert atmosphere
15.1: dmap; triethylamine; 2,4,6-trichlorobenzoyl chloride / toluene / 1.67 h / 0 - 20 °C / Inert atmosphere
With morpholine; titanium(IV) isopropylate; hydrogenchloride; tert.-butylhydroperoxide; dmap; sodium chlorite; tetrakis(triphenylphosphine) palladium(0); sodium dihydrogenphosphate dihydrate; 2-methyl-but-2-ene; oxalyl dichloride; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; diethyl (2S,3S)-tartrate; [bis(acetoxy)iodo]benzene; dimethylsulfide borane complex; 2,4,6-trichlorobenzoyl chloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; toluene; acetonitrile; benzene; 1.1: |Swern Oxidation / 1.2: |Swern Oxidation / 2.1: |Wittig Olefination / 4.1: |Sharpless Asymmetric Epoxidation / 7.1: |Wittig Olefination;
DOI:10.1002/hlca.201300255
Guidance literature:
Multi-step reaction with 3 steps
1.1: trifluoroacetic acid / dichloromethane / 1 h / 0 °C / Inert atmosphere
1.2: 4 h / 0 - 20 °C / Inert atmosphere
2.1: morpholine; tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran / 3 h / 25 °C / Inert atmosphere
3.1: dmap; triethylamine; 2,4,6-trichlorobenzoyl chloride / toluene / 1.67 h / 0 - 20 °C / Inert atmosphere
With morpholine; dmap; tetrakis(triphenylphosphine) palladium(0); 2,4,6-trichlorobenzoyl chloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; toluene;
DOI:10.1002/hlca.201300255
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1613724-91-6