1-Phenyl-2,5,8,11,14,17,20,23,26,29-decaoxatriacontane
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With hydrogen; palladium 10% on activated carbon In tetrahydrofuran for 1.08333h; | 97% |
With hydrogen; palladium 10% on activated carbon In methanol under 2.58551 Torr; | 74% |
pentaethylene glycol
2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With potassium hydroxide In tetrahydrofuran for 18h; Inert atmosphere; Reflux; | 65% |
pentaethylene glycol
3,6,9-trioxadecyl bromide
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
Stage #1: pentaethylene glycol With sodium hydride In toluene at 20℃; for 2h; Stage #2: 3,6,9-trioxadecyl bromide In toluene at 20℃; for 1h; | 51% |
3,6,9,12,15,18,21-heptaoxadocosan-1-ol
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With benzenesulfonyl chloride; benzene Erwaermen des Reaktionsprodukts mit Natrium-diaethylenglykolat in Diaethylenglykol; |
hexaethylene glycol monomethyl ether
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With sodium hydroxide; benzenesulfonyl chloride; benzene Erwaermen des Reaktionsprodukts mit Natrium-triaethylenglykolat in Triaethylenglykol; |
3,6,9,12,15-pentaoxahexadecanol
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: benzene; benzenesulfonyl chloride; sodium hydroxide / Erwaermen des Reaktionsprodukts mit Natrium-diaethylenglykolat in Diaethylenglykol 2: benzene; benzenesulfonyl chloride / Erwaermen des Reaktionsprodukts mit Natrium-diaethylenglykolat in Diaethylenglykol View Scheme |
triethylene glucol monomethyl ether
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium hydroxide; benzenesulfonyl chloride; benzene / Erwaermen des Reaktionsprodukts mit Natrium-triaethylenglykolat in Triaethylenglykol 2: sodium hydroxide; benzenesulfonyl chloride; benzene / Erwaermen des Reaktionsprodukts mit Natrium-triaethylenglykolat in Triaethylenglykol View Scheme |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
propargyl bromide
2,5,8,11,14,17,20,23,26,29-decaoxadotriacont-31-yne
Conditions | Yield |
---|---|
Stage #1: 2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol With sodium hydride In tetrahydrofuran; mineral oil Stage #2: propargyl bromide In tetrahydrofuran; mineral oil at 0 - 20℃; for 4h; | 99% |
With potassium tert-butylate In tetrahydrofuran at 0 - 20℃; for 168h; Inert atmosphere; | 34% |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
(E)-p-formylcinnamic acid
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In xylene for 4h; Heating / reflux; | 97% |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
2,5,8,11,14,17,20,23,26-nonaoxaoctacosan-28-oic acid
Conditions | Yield |
---|---|
With Jones reagent In acetone at 20℃; for 2h; | 90% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 14h; Reagent/catalyst; Solvent; Temperature; | 80% |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
p-toluenesulfonyl chloride
nonaethylene glycol methyl tosyl ether
Conditions | Yield |
---|---|
With sodium hydroxide; PEG 550 In tetrahydrofuran; water | 78% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile Heating; | 71% |
C17H12O3
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
2,5,8,11,14,17,20,23,26-nonaoxaoctacosan-28-yl 3-(4-methylphenyl)-1-oxo-1H-indene-2-carboxylate
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap In dichloromethane at 20℃; | 68% |
(E)-1,3-Bis(cyclohexylmethyl)-8-(4-(2-(1H-imidazol-1-ylcarbonyl)vinyl)phenyl)-9H-purin-2,6(1H,3H)-dione
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
(E)-4-(1,3-Bis(cyclohexylmethyl)-1,2,3,6-tetrahydro-2.6-dioxo-9H-purin-8-yl)cinnamic Acid Nonaethylene Glycol Monomethyl Ether Ester
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 18h; Heating / reflux; | 65% |
bromoacetic acid tert-butyl ester
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
Stage #1: 2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol With sodium hydride In tetrahydrofuran; mineral oil at 20℃; for 0.5h; Stage #2: bromoacetic acid tert-butyl ester In tetrahydrofuran; mineral oil at 20℃; for 1h; | 59% |
Stage #1: 2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol With sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Stage #2: bromoacetic acid tert-butyl ester In tetrahydrofuran at 20℃; for 1h; | 59% |
Stage #1: 2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol With sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Stage #2: bromoacetic acid tert-butyl ester In tetrahydrofuran at 20℃; for 1h; | 59% |
Stage #1: 2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol With sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Stage #2: bromoacetic acid tert-butyl ester In tetrahydrofuran at 20℃; for 1h; | 59% |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
4-bromomethyl pyridine hydrobromide
Conditions | Yield |
---|---|
Stage #1: 2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol With sodium hydride In tetrahydrofuran; mineral oil at 25℃; for 0.5h; Inert atmosphere; Stage #2: 4-bromomethyl pyridine hydrobromide With sodium hydride In tetrahydrofuran; mineral oil at 25℃; for 14.5h; Inert atmosphere; | 53% |
2-(1,3-Bis(cyclohexylmethyl)-1,2,3,6-tetrahydro-2,6-dioxo-9H-purin-8-yl)benzoic acid
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile Heating / reflux; | 43% |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
28-bromo-2,5,8,11,14,17,20,23,26-nonaoxaoctacosane
Conditions | Yield |
---|---|
With phosphorus tribromide In diethyl ether at 0℃; | 22% |
Multi-step reaction with 2 steps 1: triethylamine / dichloromethane / 16 h / 20 °C / Inert atmosphere 2: tetrabutylammomium bromide / acetonitrile / 16 h / 50 °C / Inert atmosphere View Scheme |
(E)-4-(1,3-Bis(cyclohexylmethyl)-1,2,3,6-tetrahydro-6-oxo-2-thioxo-9H-purin-8-yl)cinnamic Acid
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile Heating / reflux; | 20% |
3-butyl-1-chloro-isoquinoline
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
3-butyl-1-(26-methoxy-3,6,9,12,15,18,21,24-octaoxa-hexacosyloxy)-isoquinoline
Conditions | Yield |
---|---|
With sodium at 100 - 110℃; |
4-butyl-1-chloro-isoquinoline
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
4-butyl-1-(26-methoxy-3,6,9,12,15,18,21,24-octaoxa-hexacosyloxy)-isoquinoline
Conditions | Yield |
---|---|
With sodium at 100 - 110℃; |
1-chloro-3-hexylisoquinoline
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
3-hexyl-1-(26-methoxy-3,6,9,12,15,18,21,24-octaoxa-hexacosyloxy)-isoquinoline
Conditions | Yield |
---|---|
With sodium at 110℃; |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With sodium hydroxide; benzenesulfonyl chloride; benzene Beim Erwaermen des Reaktionsprodukts mit Methylamin in Aethanol; | |
Multi-step reaction with 2 steps 1: 78 percent / NaOH; PEG 550 / H2O; tetrahydrofuran 2: 96 percent / ethanol View Scheme |
(13)C6C22H34N4O4
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
toluene-4-sulfonic acid
nonaethylene glycol methyl tosyl ether
Conditions | Yield |
---|---|
In pyridine at 20℃; |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In DMF (N,N-dimethyl-formamide) at 55℃; for 20h; |
2,5,8,11,14,17,20,23,26-Nonaoxaoctacosan-28-ol
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In DMF (N,N-dimethyl-formamide) at 20 - 40℃; for 2h; |
The Nonaethylene glycol monomethyl ether with cas registry number of 6048-68-6, belongs to the following product categories: Ethylene Glycols & Monofunctional Ethylene Glycols; Monofunctional Ethylene Glycols. This chemical's molecular formula is C19H40O10 and molecular weight is 428.51.Its systematic name is 2,5,8,11,14,17,20,23,26-nonaoxaoctacosan-28-ol.
Physical properties about Nonaethylene glycol monomethyl ether are: (1)ACD/BCF (pH 5.5): 1; (2)ACD/BCF (pH 7.4): 1; (3)ACD/KOC (pH 5.5): 1; (4)ACD/KOC (pH 7.4): 1; (5)#H bond acceptors: 10; (6)#H bond donors: 1; (7)#Freely Rotating Bonds: 27; (8)Polar Surface Area: 92.3 Å2; (9)Index of Refraction: 1.453; (10)Molar Refractivity: 107.31 cm3; (11)Molar Volume: 396.9 cm3; (12)Polarizability: 42.54×10-24cm3; (13)Surface Tension: 37.4 dyne/cm; (14)Enthalpy of Vaporization: 87.15 kJ/mol; (15)Vapour Pressure: 1.17E-11 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES:O(CCOCCOCCO)CCOCCOCCOCCOCCOCCOC;
(2)InChI:InChI=1/C19H40O10/c1-21-4-5-23-8-9-25-12-13-27-16-17-29-19-18-28-15-14-26-11-10-24-7-6-22-3-2-20/h20H,2-19H2,1H3;
(3)InChIKey:VVHAVLIDQNWEKF-UHFFFAOYAD;
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