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piperidine-4-propanol

  • CAS:7037-49-2
  • purity:99%
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Details

Manufacturer supply piperidine-4-propanol 7037-49-2 with sufficient stock and high standard

  • Molecular Formula: C8H17 N O
  • Molecular Weight: 143.229
  • Vapor Pressure: 0.0091mmHg at 25°C 
  • Melting Point: 65 °C 
  • Boiling Point: 235.5°Cat760mmHg 
  • PKA: 15.16±0.10(Predicted) 
  • Flash Point: 90.2°C 
  • PSA: 32.26000 
  • Density: 0.929g/cm3 
  • LogP: 1.08730 

piperidine-4-propanol(Cas 7037-49-2) Usage

InChI:InChI=1/C8H17NO/c10-7-1-2-8-3-5-9-6-4-8/h8-10H,1-7H2

7037-49-2 Relevant articles

N-ARYL AND N-HETEROARYL PIPERIDINE DERIVATIVES AS LIVER X RECEPTOR β AGONISTS, COMPOSITIONS, AND THEIR USE

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Page/Page column 55, (2018/04/27)

Provided herein are certain substituted ...

Preparation of monoalkylpiperidines via the mild hydrogenation of monoalkynylpyridines

Usuki, Toyonobu,Komatsu, Akira

supporting information, p. 2856 - 2858 (2017/06/27)

Monoalkynylpyridines were prepared via a...

METHOD FOR PRODUCING PIPERIDINE COMPOUND

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Paragraph 0057; 0058; 0060, (2018/04/18)

PROBLEM TO BE SOLVED: To provide a metho...

9H-PYRROLO-DIPYRIDINE DERIVATIVES

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, (2016/09/22)

The invention relates to 9H-pyrrolo-dipy...

7037-49-2 Process route

4-(3-Hydroxypropyl)pyridine
2629-72-3

4-(3-Hydroxypropyl)pyridine

3-(piperidin-4-yl)propan-1-ol
7037-49-2

3-(piperidin-4-yl)propan-1-ol

Conditions
Conditions Yield
With hydrogenchloride; Adam’s catalyst; hydrogen; In methanol; water; for 46h; under 60.006 Torr; Inert atmosphere;
98%
With hydrogen; palladium on activated charcoal; In acetic acid; for 48h; under 2585.7 Torr;
95%
With hydrogen; acetic acid; 10percent Pd/C; at 20 ℃; under 2585.81 Torr;
90%
With hydrogen; Rh on carbon; In ethanol; at 60 ℃; for 24h; under 3102.89 Torr;
85%
With water; acetic acid; platinum; Hydrogenation;
With Rh/Al2O3; In methanol;
palladium-carbon; In acetic acid;
With hydrogen; 5% rhodium-on-charcoal; In water; at 50 ℃; under 15514.9 Torr;
Multi-step reaction with 3 steps
1: acetone / 1 h / 65 °C
2: sodium tetrahydroborate / water; methanol / 2 h / 0 - 90 °C
3: palladium(II) hydroxide; hydrogen / ethanol / 12 h / 50 °C
With sodium tetrahydroborate; hydrogen; palladium(II) hydroxide; In methanol; ethanol; water; acetone;
With platinum(IV) oxide; hydrogen; In acetic acid; at 40 ℃; for 24h; under 38011.4 Torr;
3-(pyridin-4-yl)propane-2-yn-1-ol
93524-95-9

3-(pyridin-4-yl)propane-2-yn-1-ol

3-(piperidin-4-yl)propan-1-ol
7037-49-2

3-(piperidin-4-yl)propan-1-ol

Conditions
Conditions Yield
With palladium 10% on activated carbon; hydrogen; In acetic acid; at 20 ℃; for 6h; under 760.051 Torr; Inert atmosphere;
43%

7037-49-2 Upstream products

  • 2629-72-3
    2629-72-3

    4-(3-Hydroxypropyl)pyridine

  • 71879-55-5
    71879-55-5

    ethyl 3-(piperid-4-yl)propionate

  • 156185-63-6
    156185-63-6

    N-Boc-piperidin-4-yl-propanol

  • 15854-87-2
    15854-87-2

    4-iodopyridine

7037-49-2 Downstream products

  • 7037-30-1
    7037-30-1

    3-(1-methylpiperidin-4-yl)propan-1-ol

  • 115482-69-4
    115482-69-4

    N-benzoyl-4-(3-hydroxypropyl)piperidine

  • 99198-80-8
    99198-80-8

    benzyl 4-(2-hydroxypropyl)-1-piperidinecarboxylate

  • 156185-63-6
    156185-63-6

    N-Boc-piperidin-4-yl-propanol