4-(2-piperidinoethoxy)aniline


  • CAS 38948-27-5
  • Purity 99%
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Buy cost-effective 99% pure 4-(2-piperidinoethoxy)aniline 38948-27-5 now

  • Molecular Formula: C13H20 N2 O
  • Molecular Weight: 220.315
  • Vapor Pressure: 6.92E-06mmHg at 25°C 
  • Melting Point: 67 °C 
  • Boiling Point: 377.1°Cat760mmHg 
  • PKA: 8.81±0.10(Predicted) 
  • Flash Point: 181.9°C 
  • PSA: 38.49000 
  • Density: 1.07g/cm3 
  • LogP: 2.65260 

4-(2-piperidinoethoxy)aniline(Cas 38948-27-5) Usage

General Description

4-(2-piperidinoethoxy)aniline, also known as N-(2-Piperidinylethoxy)aniline, is a chemical compound with a molecular formula C13H21N3O. It is a white to light brown solid that is commonly used in the synthesis of pharmaceuticals and dyes. 4-(2-piperidinoethoxy)aniline is a versatile building block for the preparation of various biologically active molecules, including antihistamines and anti-cancer agents. It is also used as an intermediate in the production of organic chemicals and can be utilized in the manufacture of veterinary drugs and agrochemicals. Additionally, 4-(2-piperidinoethoxy)aniline can be employed as a corrosion inhibitor and as a component in the formulation of surfactants and lubricants.

InChI:InChI=1/C13H20N2O/c14-12-4-6-13(7-5-12)16-11-10-15-8-2-1-3-9-15/h4-7H,1-3,8-11,14H2

38948-27-5 Relevant articles

A platinum(ii) phenylphenanthroimidazole with an extended side-chain exhibits slow dissociation from a c-kit G-quadruplex motif

Castor, Katherine J.,Liu, Zhaomin,Fakhoury, Johans,Hancock, Mark A.,Mittermaier, Anthony,Moitessier, Nicolas,Sleiman, Hanadi F.

, p. 17836 - 17845 (2013)

A series of three platinum(II) phenanthr...

Evaluation of 2-(piperidine-1-yl)-ethyl (PIP) as a protecting group for phenols: Stability to ortho-lithiation conditions and boiling concentrated hydrobromic acid, orthogonality with most common protecting group classes, and deprotection via Cope elimination or by mild Lewis acids

Norén, Rolf

, (2021/04/07)

A new protecting group, 2-(piperidine-1-...

MULTI-SUBSTITUTED PYRIMIDINE DERIVATIVES WITH EXCELLENT KINASE INHIBITORY ACTIVITIES

-

Page/Page column 0151-0152, (2019/10/29)

Disclosed are a novel pyrimidine derivat...

Design, synthesis, biological evaluation and molecular docking studies of novel 3-aryl-4-anilino-2H-chromen-2-one derivatives targeting ERα as anti-breast cancer agents

Luo, Guoshun,Chen, Mingqi,Lyu, Weiting,Zhao, Ruheng,Xu, Qian,You, Qidong,Xiang, Hua

, p. 2668 - 2673 (2017/05/29)

The estrogen receptor (ER) has played an...

Discovery of biphenyl-based VEGFR-2 inhibitors. Part 3: Design, synthesis and 3D-QSAR studies

Lu, Wen,Li, Pengfei,Shan, Yuanyuan,Su, Ping,Wang, Jinfeng,Shi, Yaling,Zhang, Jie

, p. 1044 - 1054 (2015/03/04)

VEGFR-2 plays an essential role in angio...

38948-27-5 Process route

tert-butyl ((4-(2-piperidin-1-yl)ethoxy)phenyl)carbamate
866021-30-9

tert-butyl ((4-(2-piperidin-1-yl)ethoxy)phenyl)carbamate

4-(2-(piperidin-1-yl)ethoxy)aniline
38948-27-5

4-(2-(piperidin-1-yl)ethoxy)aniline

Conditions
Conditions Yield
With trifluoroacetic acid; In dichloromethane; for 0.25h;
93%
With hydrogenchloride; In ethyl acetate; at 25 ℃; for 1h;
291.7 mg
In tetrahydrofuran; dichloromethane; at 20 ℃; for 1h;
N-chloroethylpiperidine hydrochloride
2008-75-5

N-chloroethylpiperidine hydrochloride

4-amino-phenol
123-30-8

4-amino-phenol

4-(2-(piperidin-1-yl)ethoxy)aniline
38948-27-5

4-(2-(piperidin-1-yl)ethoxy)aniline

Conditions
Conditions Yield
With sodium hydroxide; In N,N-dimethyl-formamide; at 75 ℃; for 2h;
68%

38948-27-5 Upstream products

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    92033-76-6

    1-[2-(1-piperidinyl)ethoxy]4-nitrobenzene

  • 59954-07-3
    59954-07-3

    acetic acid-[4-(2-piperidino-ethoxy)-anilide]

  • 85002-97-7
    85002-97-7

    1-(2-(4-nitrophenoxy)ethyl)piperidine hydrochloride

  • 866021-30-9
    866021-30-9

    tert-butyl ((4-(2-piperidin-1-yl)ethoxy)phenyl)carbamate

38948-27-5 Downstream products

  • 38519-98-1
    38519-98-1

    (5,6-dimethyl-benzooxazol-2-yl)-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-amine

  • 1430234-73-3
    1430234-73-3

    C30 H32 N6 O3

  • 1567327-14-3
    1567327-14-3

    2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)benzo[d][1,2]selenazol-3(2H)-one

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