• Product NameLevodropropizine
  • CasNo. 99291-25-5
  • MFC13H20N2O2
  • MW236.314
  • Purity
  • Appearancewhite solid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 99291-25-5

MF: C13H20N2O2

Appearance: white solid

Cost-effective and customizable Levodropropizine 99291-25-5 in stock

  • Molecular Formula:C13H20N2O2
  • Molecular Weight:236.314
  • Appearance/Colour:white solid 
  • Vapor Pressure:1.5E-07mmHg at 25°C 
  • Melting Point:98-100 °C 
  • Refractive Index:1.576 
  • Boiling Point:412.7 °C at 760 mmHg 
  • PKA:14.21±0.20(Predicted) 
  • Flash Point:220.9 °C 
  • PSA:46.94000 
  • Density:1.168 g/cm3 
  • LogP:0.16470 

Levodropropizine(Cas 99291-25-5) Usage

Definition

ChEBI: A member of the class of N-arylpiperazines that is N-phenylpiperazine in which the amino hydrogen is replaced by a 2,3-dihydroxypropyl group (the S-enantiomer). A peripherally acting antitussive drug t at is used as an alternative to opioids.

InChI:InChI=1/C13H20N2O2/c16-11-13(17)10-14-6-8-15(9-7-14)12-4-2-1-3-5-12/h1-5,13,16-17H,6-11H2/t13-/m0/s1

99291-25-5 Relevant articles

Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO2 with Epoxides Catalyzed by Phenol-Functionalized Phosphonium Salts

Hu, Yuya,Wei, Zhihong,Frey, Anna,Kubis, Christoph,Ren, Chang-Yue,Spannenberg, Anke,Jiao, Haijun,Werner, Thomas

, p. 363 - 372 (2020/11/30)

A series of hydroxy-functionalized phosp...

Production process of levodropropizine

-

Paragraph 0022, (2016/12/07)

The invention belongs to the technical f...

Chemo-enzymatic synthesis of levodropropizine

Caselli, Emilia,Tosi, Giovanni,Forni, Arrigo,Bucciarelli, Maria,Prati, Fabio

, p. 1029 - 1032 (2007/10/03)

Levodropropizine, an antitussive drug, w...

Process for the optical resolution of dropopizine

-

, (2008/06/13)

A process for the optical resolution of ...

99291-25-5 Process route

4-phenyl-1-piperazine
92-54-6

4-phenyl-1-piperazine

(2R)-3-chloro-1,2-propanediol
57090-45-6

(2R)-3-chloro-1,2-propanediol

levodropropizine
99291-25-5,99291-24-4

levodropropizine

Conditions
Conditions Yield
In water; at 10 - 42 ℃; for 12.5h; Temperature; Cooling with ice; Large scale;
80.6%
4-phenyl-1-piperazine
92-54-6

4-phenyl-1-piperazine

levodropropizine
99291-25-5,99291-24-4

levodropropizine

Conditions
Conditions Yield
In benzene;
In dichloromethane;
Multi-step reaction with 3 steps
1: sodium hydroxide / water / 0.25 h / 75 °C
2: (2-hydroxyphenyl)diphenyl(propyl)phosphonium iodide / neat (no solvent) / 24 h / 45 °C / 7500.75 Torr / Autoclave
3: sodium hydroxide / water / 3 h / 23 °C
With (2-hydroxyphenyl)diphenyl(propyl)phosphonium iodide; sodium hydroxide; In water;
Multi-step reaction with 3 steps
1: sodium hydroxide / water / 0.25 h / 75 °C
2: (2-hydroxyphenyl)diphenyl(propyl)phosphonium iodide / neat (no solvent) / 48 h / 23 °C / 7500.75 Torr / Autoclave
3: sodium hydroxide / water / 3 h / 23 °C
With (2-hydroxyphenyl)diphenyl(propyl)phosphonium iodide; sodium hydroxide; In water;

99291-25-5 Upstream products

  • 92-54-6
    92-54-6

    4-phenyl-1-piperazine

  • 50765-70-3
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    (S)-1-tosyloxy-2,3-propanediol

  • 113826-06-5
    113826-06-5

    (R)-glycidyl tosylate

  • 57090-45-6
    57090-45-6

    (2R)-3-chloro-1,2-propanediol

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