53786-28-0

  • Product Name5-Chloro-1-(4-piperidyl)-2-benzimidazolinone
  • Molecular FormulaC12H14ClN3O
  • Molecular Weight251.716
  • Purity99%
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Product Details

Quick Details

  • CasNo: 53786-28-0
  • Molecular Formula: C12H14ClN3O
  • Purity: 99%

Manufacturer supply top purity 5-Chloro-1-(4-piperidyl)-2-benzimidazolinone 53786-28-0 with ISO standards

  • Molecular Formula:C12H14ClN3O
  • Molecular Weight:251.716
  • Vapor Pressure:0Pa at 20℃ 
  • Melting Point:228-231 °C(lit.) 
  • Refractive Index:1.605 
  • PKA:11.12±0.30(Predicted) 
  • PSA:49.82000 
  • Density:1.323 g/cm3 
  • LogP:2.23630 

5-Chloro-1-(4-piperidyl)-2-benzimidazolinone(Cas 53786-28-0) Usage

Flammability and Explosibility

Notclassified

General Description

5-Chloro-1-(4-piperidyl)-2-benzimidazolinone is a 2-benzimidazolone derivative. It exhibits anti-nauseant properties.

InChI:InChI=1/C12H14ClN3O/c13-8-1-2-11-10(7-8)15-12(17)16(11)9-3-5-14-6-4-9/h1-2,7,9,14H,3-6H2,(H,15,17)

53786-28-0 Relevant articles

Optimization of a Series of Mu Opioid Receptor (MOR) Agonists with High G Protein Signaling Bias

Kennedy, Nicole M.,Schmid, Cullen L.,Ross, Nicolette C.,Lovell, Kimberly M.,Yue, Zhizhou,Chen, Yen Ting,Cameron, Michael D.,Bohn, Laura M.,Bannister, Thomas D.

, p. 8895 - 8907 (2018/10/05)

While mu opioid receptor (MOR) agonists ...

NOVEL 1,3-DIHYDRO-BENZOIMIDAZOL-2-ONES AS M1 AGONISTS

-

Page/Page column 34, (2009/11/29)

The present invention relates to novel M...

NOVEL PIPERIDINYL-1,3-DIHYDRO-BENZOIMIDAZOL-2-ONES AS M1 AGONISTS

-

Page/Page column 35, (2009/11/29)

The present invention relates to novel M...

Benzodiazepine calcitonin gene-related peptide (CGRP) receptor antagonists: Optimization of the 4-substituted piperidine

Burgey, Christopher S.,Stump, Craig A.,Nguyen, Diem N.,Deng, James Z.,Quigley, Amy G.,Norton, Beth R.,Bell, Ian M.,Mosser, Scott D.,Salvatore, Christopher A.,Rutledge, Ruth Z.,Kane, Stefanie A.,Koblan, Kenneth S.,Vacca, Joseph P.,Graham, Samuel L.,Williams, Theresa M.

, p. 5052 - 5056 (2007/10/03)

In our continuing effort to identify CGR...

53786-28-0 Process route

4-(5-chloro-2-oxo-2,3-dihydro-benzoimidazol-1-yl)-piperidine-1-carboxylic acid ethyl ester
53786-46-2

4-(5-chloro-2-oxo-2,3-dihydro-benzoimidazol-1-yl)-piperidine-1-carboxylic acid ethyl ester

5-chloro-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one
53786-28-0

5-chloro-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one

Conditions
Conditions Yield
With sodium hydroxide; for 8h; Heating;
96%
With sodium hydroxide; at 100 ℃;
With ammonium chloride; In water;
4-(4-chloro-2-nitro-anilino)-piperidine-1-carboxylic acid ethyl ester
53786-44-0

4-(4-chloro-2-nitro-anilino)-piperidine-1-carboxylic acid ethyl ester

5-chloro-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one
53786-28-0

5-chloro-1-(piperidin-4-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: Zn; aq. HCl / methanol / 50 °C
2: acetonitrile
3: aq. NaOH / 100 °C
With hydrogenchloride; sodium hydroxide; zinc; In methanol; acetonitrile;
Multi-step reaction with 3 steps
1: 93 percent / H2 / Raney Ni / ethanol; tetrahydrofuran / 1 h / Ambient temperature
2: 90 percent / Et3N / CH2Cl2 / 0.5 h / 0 °C
3: 96 percent / 10percent NaOH / 8 h / Heating
With sodium hydroxide; hydrogen; triethylamine; nickel; In tetrahydrofuran; ethanol; dichloromethane;

53786-28-0 Upstream products

  • 53786-46-2
    53786-46-2

    4-(5-chloro-2-oxo-2,3-dihydro-benzoimidazol-1-yl)-piperidine-1-carboxylic acid ethyl ester

  • 58859-46-4
    58859-46-4

    ethyl 4-aminopiperidine-1-carboxylate

  • 53786-45-1
    53786-45-1

    ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate

  • 53786-44-0
    53786-44-0

    4-(4-chloro-2-nitro-anilino)-piperidine-1-carboxylic acid ethyl ester

53786-28-0 Downstream products

  • 85076-06-8
    85076-06-8

    axamozide

  • 95017-57-5
    95017-57-5

    1-(1-{3-[Bis-(4-fluoro-phenyl)-amino]-propyl}-piperidin-4-yl)-5-chloro-1,3-dihydro-benzoimidazol-2-one

  • 85494-56-0
    85494-56-0

    1-[1-(4-(4-fluorophenyl)-tetrahydro-2-furylmethyl)-4-piperidyl]-5-chloro-benzimidazolin-2-one maleate

  • 58859-90-8
    58859-90-8

    5-chloro-1-{1-[4-(4-fluoro-phenyl)-4-phenyl-butyl]-piperidin-4-yl}-1,3-dihydro-benzoimidazol-2-one

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