104-29-0

  • Product Name:Chlorphenesin
  • Molecular Formula:C9H11ClO3
  • Purity:99%
  • Molecular Weight:202.638
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Product Details

pd_meltingpoint:77-79 °C

Appearance:white to off-white crystalline powder

Export Top Purity Chlorphenesin 104-29-0 In Stock

  • Molecular Formula:C9H11ClO3
  • Molecular Weight:202.638
  • Appearance/Colour:white to off-white crystalline powder 
  • Vapor Pressure:4.13E-06mmHg at 25°C 
  • Melting Point:77-79 °C 
  • Refractive Index:1.565 
  • Boiling Point:369.45 °C at 760 mmHg 
  • PKA:13.44±0.20(Predicted) 
  • Flash Point:177.237 °C 
  • PSA:49.69000 
  • Density:1.318 g/cm3 
  • LogP:1.07200 

Chlorphenesin(Cas 104-29-0) Usage

Definition

ChEBI: Glycerol in which the hydrogen of one of the primary hydroxy groups is substituted by a 4-chlorophenyl group. It has antifungal and antibacterial properties, and is used for treatment of cutaneous and vaginal infections. Its 1-carbamate is used as a skelet l muscle relaxant for the treatment of painful muscle spasm.

Brand name

Maolate (Pharmacia & Upjohn).

Flammability and Explosibility

Notclassified

InChI:InChI=1/C9H11ClO3/c10-7-1-3-9(4-2-7)13-6-8(12)5-11/h1-4,8,11-12H,5-6H2/t8-/m0/s1

104-29-0 Relevant articles

A New and Efficient Heterogeneous System for the Oxidative Cleavage of 1,2-Diols and the Oxidation of Hydroquinones

Daumas, M.,Vo-Quang, Y.,Vo-Quang, L.,Goffic, F. Le

, p. 64 - 65 (1989)

Sodium periodate/wet silica gel in the p...

One-pot synthesis of aryloxypropanediols from glycerol: Towards valuable chemicals from renewable sources

Truscello, Ada M.,Gambarotti, Cristian,Lauria, Mirvana,Auricchio, Sergio,Leonardi, Gabriella,Shisodia, Suresh U.,Citterio, Attilio

, p. 625 - 628 (2013)

Glycerol offers an easy and green route ...

Kinetics and mechanism of degradation of chlorphenesin carbamate in strongly acidic aqueous solutions

Hara,Hayashi,Yoshida

, p. 3481 - 3484 (1986)

-

Ligand-Free Copper-Catalyzed Ullmann-Type C?O Bond Formation in Non-Innocent Deep Eutectic Solvents under Aerobic Conditions

Capriati, Vito,García-álvarez, Joaquín,Marinò, Manuela,Perna, Filippo M.,Quivelli, Andrea Francesca,Vitale, Paola

, (2021/12/09)

An efficient and novel protocol was deve...

Exploration of the expeditious potential of Pseudomonas fluorescens lipase in the kinetic resolution of racemic intermediates and its validation through molecular docking

Soni, Surbhi,Dwivedee, Bharat P.,Sharma, Vishnu K.,Patel, Gopal,Banerjee, Uttam C.

, p. 85 - 94 (2017/12/26)

A profoundly time-efficient chemoenzymat...

Method for green, efficient and selective synthesis of chlorphenesin

-

Paragraph 0028-0043, (2018/09/13)

The invention discloses a method for gre...

A synthesis method of chlorphenesin

-

Paragraph 0082; 0083, (2017/09/01)

The invention relates to a synthetic met...

104-29-0 Process route

3-(p-chlorophenoxy)-1,2-propanediol-2-carbamate
61514-96-3

3-(p-chlorophenoxy)-1,2-propanediol-2-carbamate

chlorphenesin carbamate
886-74-8,126632-50-6

chlorphenesin carbamate

chlorphenesin
104-29-0

chlorphenesin

Conditions
Conditions Yield
With sodium hydroxide; In water; at 0 ℃; Rate constant; degradation was studied;
 
4-chloro-phenol
106-48-9,82344-39-6

4-chloro-phenol

3-monochloro-1,2-propanediol
96-24-2

3-monochloro-1,2-propanediol

chlorphenesin
104-29-0

chlorphenesin

Conditions
Conditions Yield
With tetrabutylammomium bromide; sodium hydroxide; at 105 ℃; for 3h; Concentration; Reagent/catalyst;
95.1%
With sodium hydroxide; In ethanol; for 2h; Heating;
81%
With alkali;
 
With sodium ethanolate;
 
With potassium carbonate; Yield given. Multistep reaction; 1.) CH3CN, reflux, 1 h, 2.) reflux, overnight;
 
With potassium carbonate; Yield given. Multistep reaction; 1.) acetonitrile, reflux, 1 h, 2.) reflux, overnight;
 

104-29-0 Upstream products

  • 106-48-9
    106-48-9

    4-chloro-phenol

  • 96-24-2
    96-24-2

    3-monochloro-1,2-propanediol

  • 62067-19-0
    62067-19-0

    2-Benzyloxy-3-(4-chloro-phenoxy)-propan-1-ol

  • 2212-05-7
    2212-05-7

    4-chlorophenyl 2,3-epoxypropyl ether

104-29-0 Downstream products

  • 39735-79-0
    39735-79-0

    1-chloro-3-(4-chloro-phenoxy)-propan-2-ol

  • 43018-72-0
    43018-72-0

    p-chlorophenoxyacetaldehyde

  • 23958-75-0
    23958-75-0

    Chloro-acetic acid 3-(4-chloro-phenoxy)-2-hydroxy-propyl ester

  • 23958-86-3
    23958-86-3

    Chloro-acetic acid 1-(2-chloro-acetoxymethyl)-2-(4-chloro-phenoxy)-ethyl ester

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