145108-58-3

  • Product NameDexmedetomidine hydrochloride
  • Molecular FormulaC13H16N2.HCl
  • Molecular Weight236.744
  • Purity99%
  • AppearanceWhite or almost white crystalline powder
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Product Details

Quick Details

  • CasNo: 145108-58-3
  • Molecular Formula: C13H16N2.HCl
  • Appearance: White or almost white crystalline powder
  • Purity: 99%

Manufacturer supply high quality Dexmedetomidine hydrochloride 145108-58-3 with GMP standards

  • Molecular Formula:C13H16N2*ClH
  • Molecular Weight:236.744
  • Appearance/Colour:White or almost white crystalline powder 
  • Vapor Pressure:1.08E-05mmHg at 25°C 
  • Melting Point:153 - 158oC 
  • Boiling Point:381.9 ºC at 760 mmHg 
  • Flash Point:191.3 ºC 
  • PSA:28.68000 
  • Density:1.17 g/cm3 
  • LogP:3.98030 

4-((S)-alpha,2,3-Trimethylbenzyl)imidazole monohydrochloride(Cas 145108-58-3) Usage

Biological Activity

Active isomer of Medetomide (4-[1-(2,3-Dimethylphenyl)ethyl]-1H-imidazolehydrochloride ), a potent, highly selective α 2 -adrenoceptor agonist (K i values are 1.08 and 1750 nM for α 2 - and α 1 -adrenoceptors respectively). Displays greater selectivity over α 1 -adrenoceptors than clonidine and UK 14,304 (1620-, 220- and 300-fold respectively). Active in vivo ; displays hypotensive, bradycardic, sedative, anxiolytic, hypothermic and analgesic effects.

Biochem/physiol Actions

Dexmedetomidine hydrochloride is a highly potent and selective α2-adrenergic agonist with analgesic and sedative properties, the (+)-isomer of medetomidine. Dexmedetomidine hydrochloride is used clinically as an anesthetic agent to reduce anxiety and tension and promote relaxation and sedation without causing respiratory depression.

Brand name

Precedex

InChI:InChI=1/C13H16N2.ClH/c1-9-5-4-6-12(10(9)2)11(3)13-7-14-8-15-13;/h4-8,11H,1-3H3,(H,14,15);1H/t11-;/m0./s1

145108-58-3 Relevant articles

Preparation method of dexmedetomidine hydrochloride

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, (2020/06/20)

The invention discloses a preparation me...

Method for synthesizing dexmedetomidine hydrochloride

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, (2019/04/26)

The invention belongs to the technical f...

Industrial preparation method of dexmedetomidine hydrochloride

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, (2017/08/28)

The invention discloses an industrial pr...

Method for preparing dexmedetomidine and intermediate thereof

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, (2017/04/03)

The invention provides a method for prep...

145108-58-3 Process route

4-<1-(2,3-dimethylphenyl)-1-hydroxyethyl>-1-(triphenylmethyl)imidazole
176721-03-2

4-<1-(2,3-dimethylphenyl)-1-hydroxyethyl>-1-(triphenylmethyl)imidazole

(-)-(R)-4-(1-[2,3-dimethylphenyl]ethyl)-1H-imidazole hydrochloride
145108-58-3

(-)-(R)-4-(1-[2,3-dimethylphenyl]ethyl)-1H-imidazole hydrochloride

Conditions
Conditions Yield
Multi-step reaction with 4 steps
1: triethylsilane; trifluoroacetic acid / dichloromethane / 5 h / -10 - 20 °C
2: hydrogen; palladium 10% on activated carbon
3: ethanol / 20 °C
4: sodium hydroxide / water / pH 8.5
With triethylsilane; palladium 10% on activated carbon; hydrogen; trifluoroacetic acid; sodium hydroxide; In ethanol; dichloromethane; water;
tert-butyl 4-[1-(2,3-dimethylphenyl)-1-hydroxyethyl]-1H-imidazole-1-carboxylate

tert-butyl 4-[1-(2,3-dimethylphenyl)-1-hydroxyethyl]-1H-imidazole-1-carboxylate

(-)-(R)-4-(1-[2,3-dimethylphenyl]ethyl)-1H-imidazole hydrochloride
145108-58-3

(-)-(R)-4-(1-[2,3-dimethylphenyl]ethyl)-1H-imidazole hydrochloride

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: hydrogen; palladium 10% on activated carbon
2: ethanol / 20 °C
3: sodium hydroxide / water / pH 8.5
With palladium 10% on activated carbon; hydrogen; sodium hydroxide; In ethanol; water;

145108-58-3 Upstream products

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    1-(1-chloroethyl)-2,3-dimethylbenzene

  • 176721-03-2
    176721-03-2

    4-<1-(2,3-dimethylphenyl)-1-hydroxyethyl>-1-(triphenylmethyl)imidazole

  • 850716-46-0
    850716-46-0

    tert-butyl 4-acetyl-1H-imidazole-1-carboxylate

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