69559-11-1
- Product Name：5-(N-Ethyl-N-2-hydroxyethylamino)-2-pentylamine
- Structural Formula：
- Purity：99%
- Molecular Weight：
Product Details
Hot Sale Pharmaceutical Grade 5-(N-Ethyl-N-2-hydroxyethylamino)-2-pentylamine 69559-11-1 supplier
- Molecular Formula:C9H22N2O
- Molecular Weight:174.286
- Vapor Pressure:0.00143mmHg at 25°C
- Refractive Index:1.470-1474
- Boiling Point:263.6 °C at 760 mmHg
- PKA:14.76±0.10(Predicted)
- Flash Point:113.2 °C
- PSA：49.49000
- Density:0.937 g/cm3
- LogP:1.12830
5-(N-Ethyl-N-2-hydroxyethylamino)-2-pentylamine (Cas 69559-11-1) Usage
|
Uses |
5-(N-Ethyl-N-2-hydroxyethylamino)-2-pentylamine is a colorless and pure liquid that can be used as a pharmaceutical intermediate. |
InChI:InChI=1/C9H22N2O/c1-3-11(7-8-12)6-4-5-9(2)10/h9,12H,3-8,10H2,1-2H3
69559-11-1 Relevant articles
Method for continuously producing 5-(N-ethyl-N-2-hydroxyethyl amine)-2-pentylamine
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Paragraph 0045-0058, (2020/08/09)
The invention discloses a method for con...
Application of chiral chloroquine, hydroxychloroquine or salt of the chiral chloroquine and hydroxychloroquine as anti-coronavirus drug target 3CL hydrolase inhibitor for reducing cardiotoxicity
-
Paragraph 0120; 0126-0127, (2020/11/02)
The invention discloses an application o...
HIGH-YIELDING CONTINUOUS FLOW SYNTHESIS OF ANTIMALARIAL DRUG HYDROXYCHLOROQUINE
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Page/Page column 20-21; 18; 16, (2019/09/12)
Cost effective, semi-continuous flow met...
High-yielding continuous-flow synthesis of antimalarial drug hydroxychloroquine
Yu, Eric,Mangunuru, Hari P.R.,Telang, Nakul S.,Kong, Caleb J.,Verghese, Jenson,Gilliland, Stanley E.,Ahmad, Saeed,Dominey, Raymond N.,Gupton, B. Frank
, p. 583 - 592 (2018/03/21)
Numerous synthetic methods for the conti...
69559-11-1 Process route
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- 74509-79-8
5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone
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- 69559-11-1
rac-5-
Conditions
| Conditions | Yield |
|---|---|
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With aluminum(III) nitrate nonahydrate; magnesium(II) nitrate hexahydrate; nickel(II) nitrate hexahydrate; yttrium(lll) nitrate hexahydrate; hydrogen; sodium carbonate; sodium hydroxide; In ethanol; ammonia; water; at 80 - 400 ℃; under 4500.45 Torr; Reagent/catalyst; Temperature; Pressure; Solvent; liquid NH3;
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95.9% |
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With methanol; ammonia; und Hydrierung der hergestellten Reaktiongemisches an Raney-Nickel bei 70 at;
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Multi-step reaction with 2 steps
1: potassium carbonate; hydroxylamine / tetrahydrofuran / 0.17 h / 100 °C / Inert atmosphere; Flow reactor
2: hydrogen / tetrahydrofuran / 4 h / 80 °C / 7500.75 Torr / Inert atmosphere; Flow reactor
With hydrogen; hydroxylamine; potassium carbonate; In tetrahydrofuran;
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-
- 159346-86-8
R(-)-5-
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- 69559-11-1
rac-5-
Conditions
| Conditions | Yield |
|---|---|
|
With nickel; In toluene; at 70 ℃; for 12h;
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97% |
69559-11-1 Upstream products
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74509-79-8
5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone
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3695-29-2
5-iodo-2-pentanone
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517-23-7
3-acetyl-2-oxo-4,5-dihydrofuran
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159346-86-8
R(-)-5-
69559-11-1 Downstream products
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137433-23-9
(R)-Hydroxychloroquine
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137433-23-9
(S)-Hydroxychloroquine
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118-42-3
hydroxychloroquine
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747-36-4
Plaquenil
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