C₃₀H₃₉N₃O₄

Base Information

Chemical Name:C₃₀H₃₉N₃O₄
CAS No.:141521-28-0
Molecular Formula:C₃₀H₃₉N₃O₄
Molecular Weight:505.657
Hs Code.:

C<sub>30</sub>H<sub>39</sub>N<sub>3</sub>O<sub>4</sub>

Synonyms:C₃₀H₃₉N₃O₄

Suppliers and Price of C₃₀H₃₉N₃O₄

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 C₃₀H₃₉N₃O₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₀H₃₉N₃O₄

There total 14 articles about C₃₀H₃₉N₃O₄ 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: 85.0%

: 141538-64-9,144666-13-7
(9S,11S)-11-(4-Dimethylamino-2-methoxy-phenyl)-9-((S)-2-formyl-2-hydroxy-butyl)-5,8,9,10,11,12-hexahydro-6H-7,12-diaza-cyclonona[a]indene-7,11-dicarboxylic acid 11-methyl ester 7-(4-nitro-benzyl) ester

: 141521-28-0
C₃₀H₃₉N₃O₄

Guidance literature:: With hydrogen; palladium on activated charcoal;
DOI:10.1016/S0040-4039(00)91570-3

Reference yield:

: 121464-71-9
(R)-(2-ethoxyoxiran-2-yl)methanol

: 141521-28-0
C₃₀H₃₉N₃O₄

Guidance literature:: Multi-step reaction with 12 steps

1: 1.0N aq.NaOH / dioxane / Heating

2: H₃O+

3: 94 percent / MCPBA

4: 1) Ac2O, NaOAc, 2) K2CO3 / 1) Δ, 2) MeOH, Δ

5: 80 percent / Sn(OTf)2, N-ethylpiperidine / tetrahydrofuran

6: 97 percent / NEt₃

7: 93 percent / DBU / CH₂Cl₂

8: Raney nickel

9: 73 percent / 2,6-di-tert-butyl-4-methylpyridine / nitromethane / 96 h / 23 °C

10: 73 percent / H₃O+

11: 81 percent / SO₃, pyridine

12: 85 percent / H₂ / 10percent Pd-C

With 1-ethyl-piperidine; pyridine; sodium hydroxide; tin(II) trifluoromethanesulfonate; 2,6-di-tert-butyl-4-methylpyridine; oxonium; sulfur trioxide; hydrogen; sodium acetate; acetic anhydride; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; nickel; In tetrahydrofuran; 1,4-dioxane; nitromethane; dichloromethane;
DOI:10.1016/S0040-4039(00)91570-3

Reference yield:

: 141521-24-6
(+)-(9R,2'S)-3-thioxo-9-(methoxycarbonyl)-2-(2'-ethyl-2',3'dihydroxypropenyl)hexahydroindolizino<8,7-b>indole cyclohexylidene ketal

: 141521-28-0
C₃₀H₃₉N₃O₄

Guidance literature:: Multi-step reaction with 5 steps

1: Raney nickel

2: 73 percent / 2,6-di-tert-butyl-4-methylpyridine / nitromethane / 96 h / 23 °C

3: 73 percent / H₃O+

4: 81 percent / SO₃, pyridine

5: 85 percent / H₂ / 10percent Pd-C

With pyridine; 2,6-di-tert-butyl-4-methylpyridine; oxonium; sulfur trioxide; hydrogen; palladium on activated charcoal; nickel; In nitromethane;
DOI:10.1016/S0040-4039(00)91570-3