82424-53-1

  • Product Name:(Z,E)-2-(4-METHOXYPHENYL)([((4-METHYLPHENYL)SULPHONYL)OXY]IMINO)ACETONITRILE
  • Molecular Formula:C16H14 N2 O4 S
  • Purity:99%
  • Molecular Weight:330.364
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Product Details

Reliable Quality (Z,E)-2-(4-METHOXYPHENYL)([((4-METHYLPHENYL)SULPHONYL)OXY]IMINO)ACETONITRILE 82424-53-1 Hot Sale with Chinese Manufacturer

  • Molecular Formula:C16H14N2O4S
  • Molecular Weight:330.364
  • Vapor Pressure:1.17E-05mmHg at 25°C 
  • Boiling Point:369.7°C at 760 mmHg 
  • Flash Point:177.4°C 
  • PSA:97.13000 
  • Density:1.155g/cm3 
  • LogP:3.71758 

(Z,E)-2-(4-METHOXYPHENYL)([((4-METHYLPHENYL)SULPHONYL)OXY]IMINO)ACETONITRILE(Cas 82424-53-1) Usage

General Description

The chemical compound "(Z,E)-2-(4-METHOXYPHENYL)([((4-METHYLPHENYL)SULPHONYL)OXY]IMINO)ACETONITRILE" is a complex organic molecule with a long, specific name. It consists of a central acetonitrile group attached to a 4-methoxyphenyl and a 4-methylphenyl sulfonyloxyimino group. The compound can exist in two different geometric configurations, referred to as Z and E isomers. This chemical may have potential applications in organic synthesis and pharmaceutical research due to its unique structure and functional groups. Additionally, it may have biological activity or serve as a building block for the synthesis of other compounds. Further research and experimentation may be required to fully understand the properties and potential uses of this complex molecule.

InChI:InChI=1/C14H12N2/c15-11-14(12-7-3-1-4-8-12)16-13-9-5-2-6-10-13/h1-10,14,16H/t14-/m0/s1

82424-53-1 Relevant articles

Synthesis and anti-mitotic activity of 6,7-dihydro-4H-isothiazolo[4,5-b]pyridin-5-ones: In vivo and cell-based studies

Semenov, Victor V.,Lichitsky, Boris V.,Komogortsev, Andrey N.,Dudinov, Arkady A.,Krayushkin, Mikhail M.,Konyushkin, Leonid D.,Atamanenko, Olga P.,Karmanova, Irina B.,Strelenko, Yuri A.,Shor, Boris,Semenova, Marina N.,Kiselyov, Alex S.

, p. 573 - 585 (2016/10/12)

A series of 3,7-diaryl-6,7-dihydroisothi...

82424-53-1 Process route

p-methoxybenzylnitrile
104-47-2

p-methoxybenzylnitrile

-2-(4-methoxyphenyl)-2-[(4-methylphenylsulfonyl)oxyimino]acetonitrile
82424-53-1

-2-(4-methoxyphenyl)-2-[(4-methylphenylsulfonyl)oxyimino]acetonitrile

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: isopentyl nitrite; sodium methylate / methanol / 1 h / 5 °C
2: N,N-dimethyl-formamide / 0.25 h / 75 °C
With sodium methylate; isopentyl nitrite; In methanol; N,N-dimethyl-formamide;
p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

C<sub>9</sub>H<sub>7</sub>N<sub>2</sub>O<sub>2</sub><sup>(1-)</sup>*Na<sup>(1+)</sup>

C9H7N2O2(1-)*Na(1+)

-2-(4-methoxyphenyl)-2-[(4-methylphenylsulfonyl)oxyimino]acetonitrile
82424-53-1

-2-(4-methoxyphenyl)-2-[(4-methylphenylsulfonyl)oxyimino]acetonitrile

Conditions
Conditions Yield
In N,N-dimethyl-formamide; at 75 ℃; for 0.25h;

82424-53-1 Upstream products

  • 98-59-9
    98-59-9

    p-toluenesulfonyl chloride

  • 104-47-2
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    p-methoxybenzylnitrile