4-AMINO-1-PIPERIDINE-ETHANOL
Base Information
- Chemical Name: 4-AMINO-1-PIPERIDINE-ETHANOL
- CAS No.: 89850-72-6
Buy cost-effective 99% pure 4-AMINO-1-PIPERIDINE-ETHANOL 89850-72-6 now
- Molecular Formula: C7H16N2O
- Molecular Weight: 144.217
- Boiling Point: 250.4 °C at 760 mmHg
- Flash Point: 105.3 °C
- PSA： 49.49000
- Density: 1.028 g/cm3
- LogP: 0.04000
89850-72-6 Relevant articles
NOVEL COMPOUND HAVING ANGIOGENESIS INHIBITORY ACTIVITY, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME
-
Paragraph 0083; 0085, (2014/07/23)
Disclosed are an anti-angiogenic compoun...
Novel Compound Having Angiogenesis Inhibitory Activity, Method for Preparing Same, and Pharmaceutical Composition Comprising Same
-
Paragraph 0197; 0200, (2014/09/29)
Disclosed are an anti-angiogenic compoun...
GAS CAPTURE PROCESS
-
Page/Page column 50, (2012/11/07)
A process for the capture of CO2 from ga...
Synthesis and evaluation of novel radioiodinated benzamides for malignant melanoma
Pham, Tien Q.,Greguric, Ivan,Liu, Xiang,Berghofer, Paula,Ballantyne, Patrice,Chapman, Janette,Mattner, Filomena,Dikic, Branko,Jackson, Timothy,Loc'h, Christian,Katsifis, Andrew
, p. 3561 - 3572 (2008/02/09)
The imaging potential of a series of [12...
89850-72-6 Process route
-
-
51527-83-4
Br(1-) *C7 H11 N2 O(1+)
-
-
89850-72-6
4-amino-1-(2-hydroxyethyl)piperidine
| Conditions | Yield |
|---|---|
|
Br(1-)*C7H11N2O(1+);
With
hydrogen; sodium;
rhodium contaminated with carbon;
In
methanol;
at 60 ℃;
under 7240.26 Torr;
In
methanol;
Reflux;
|
69%
|
-
![[1-(2-hydroxyethyl)-piperidin-4-yl]-carbamic acid tert-butyl ester](/upload/2026/10/11e87c5c43394a66b9790c339dccacef_64bfc769-a859-4f3d-8cff-954f37bcdb25.png)
-
558443-53-1
[1-(2-hydroxyethyl)-piperidin-4-yl]-carbamic acid tert-butyl ester
-
-
89850-72-6
4-amino-1-(2-hydroxyethyl)piperidine
| Conditions | Yield |
|---|---|
|
With
trifluoroacetic acid;
at 20 ℃;
for 1h;
|
95%
|
|
With
hydrogenchloride;
In
ethanol; water;
for 2h;
Reflux;
|
95%
|
|
With
hydrogenchloride;
In
ethanol;
for 2h;
Reflux;
|
95%
|
|
[1-(2-hydroxyethyl)-piperidin-4-yl]-carbamic acid tert-butyl ester;
With
trifluoroacetic acid;
With
hydrogenchloride;
In
methanol;
at 20 ℃;
for 0.5h;
With
sodium hydroxide;
In
water;
at 20 ℃;
for 0.25h;
pH=> 10;
Cooling with ice;
|
87%
|
89850-72-6 Upstream products
-
558443-53-1
[1-(2-hydroxyethyl)-piperidin-4-yl]-carbamic acid tert-butyl ester
-
73874-95-0
(piperidin-4-yl)carbamic acid tert-butyl ester
-
504-24-5
4-aminopyridine
-
51527-83-4
Br(1-) *C7 H11 N2 O(1+)
89850-72-6 Downstream products
-
1201694-09-8
4-amino-N-[1-(2-hydroxy-ethyl)-piperidin-4-yl]-3-methoxy-benzamide
-
1345437-78-6
C30 H29 F2 N7 O3
-
1401732-38-4
2-(4-((6-(1-(4-methoxybenzyl)-3-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)pyrazin-2-yl)amino)piperidin-1-yl)ethanol