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Factory Sells Best Quality [(3,4,5-trimethoxyphenoxy)methyl]oxirane 74760-14-8 with steady supply

  • Molecular Formula:C12H16 O5
  • Molecular Weight:240.256
  • Vapor Pressure:8.06E-05mmHg at 25°C 
  • Boiling Point:351.9°C at 760 mmHg 
  • Flash Point:145.9°C 
  • PSA:49.45000 
  • Density:1.167g/cm3 
  • LogP:1.49000 

[(3,4,5-trimethoxyphenoxy)methyl]oxirane(Cas 74760-14-8) Usage

General Description

[(3,4,5-trimethoxyphenoxy)methyl]oxirane is a chemical compound with the molecular formula C13H16O5. It consists of a phenolic group with three methoxy substituents attached to a glycidyl ether moiety. [(3,4,5-trimethoxyphenoxy)methyl]oxirane is commonly used as a reagent in organic synthesis reactions due to its ability to act as a reactive intermediate, particularly in the reaction with nucleophiles. It is also utilized in the preparation of various pharmaceuticals and agrochemicals. Additionally, [(3,4,5-trimethoxyphenoxy)methyl]oxirane has been studied for potential applications in material science and polymer chemistry. However, it is important to handle this compound with caution as it is considered to be a potentially hazardous chemical.

InChI:InChI=1/C12H16O5/c1-13-10-4-8(16-6-9-7-17-9)5-11(14-2)12(10)15-3/h4-5,9H,6-7H2,1-3H3

74760-14-8 Relevant articles

A simple and efficient asymmetric synthesis of anxiolytic drug enciprazine

Narsaiah, A. Venkat,Nagaiah

experimental part, p. 2705 - 2707 (2010/10/18)

A straightforward and efficient asymmetr...

Chemistry and Pharmacology of the Non-Benzodiazepine Anxiolytic Enciprazine and Related Compounds

Engel, Juergen,Fleischhauer, Ilona,Jakovlev, Vladimir,Kleemann, Axel,Kutscher, Bernhard,et al.

, p. 2976 - 2981 (2007/10/02)

In the course of studies on tranquilizer...

Cardioselective aryloxy- and arylthio- hydroxypropylene-piperazinyl acetanilides which affect calcium entry

-

, (2008/06/13)

Novel compounds of the general formula S...

74760-14-8 Process route

3,4,5-trimethoxyphenol
642-71-7

3,4,5-trimethoxyphenol

epichlorohydrin
106-89-8,24969-06-0,13403-37-7

epichlorohydrin

1-(3,4,5-trimethoxyphenoxy)-2,3-epoxypropane
74760-14-8

1-(3,4,5-trimethoxyphenoxy)-2,3-epoxypropane

Conditions
Conditions Yield
With tetrabutylammomium bromide; potassium carbonate; In acetonitrile; at 20 ℃; Reflux;
90%
With sodium hydroxide; for 1h; Heating;
80%
1-(3,4,5-trimethoxyphenoxy)-2,3-epoxypropane
74760-14-8

1-(3,4,5-trimethoxyphenoxy)-2,3-epoxypropane

Conditions
Conditions Yield

74760-14-8 Upstream products

  • 642-71-7
    642-71-7

    3,4,5-trimethoxyphenol

  • 106-89-8
    106-89-8

    epichlorohydrin

74760-14-8 Downstream products

  • 68576-86-3
    68576-86-3

    Enciprazine

  • 74760-02-4
    74760-02-4

    1-[4-(2-methylsulfanyl-phenyl)-piperazin-1-yl]-3-(3,4,5-trimethoxy-phenoxy)-propan-2-ol

  • 74760-01-3
    74760-01-3

    1-[4-(2-ethoxy-phenyl)-piperazin-1-yl]-3-(3,4,5-trimethoxy-phenoxy)-propan-2-ol

  • 74760-12-6
    74760-12-6

    1-(3,4,5-trimethoxyphenoxy)-3-<4-(2-nitrophenyl)piperazinyl>propan-2-ol

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