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2-HYDROXYIMINO-2-(PHENYLSULFONYL)ACETONITRILE, a chemical compound with the molecular formula C9H8N2O3S, is a nitronyl nitroxide radical. It is known for its potential applications in various scientific fields due to its unique structure and properties. 2-HYDROXYIMINO-2-(PHENYLSULFONYL)ACETONITRILE has been studied for its use in organic synthesis, as a spin label in electron paramagnetic resonance (EPR) spectroscopy, and in the preparation of chiral auxiliaries. Additionally, as a nitroxide radical, it has the potential to function as an antioxidant, with research exploring its role in protecting cells from oxidative stress.

74755-16-1

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74755-16-1 Usage

Uses

Used in Organic Synthesis:
2-HYDROXYIMINO-2-(PHENYLSULFONYL)ACETONITRILE is used as a reagent in organic synthesis for its ability to facilitate specific chemical reactions, contributing to the formation of desired products with enhanced efficiency and selectivity.
Used as a Spin Label in EPR Spectroscopy:
In the field of biochemistry and molecular biology, 2-HYDROXYIMINO-2-(PHENYLSULFONYL)ACETONITRILE serves as a spin label, which is utilized in electron paramagnetic resonance (EPR) spectroscopy. This application allows researchers to probe the local environment and dynamics of molecules, providing insights into molecular structure and function.
Used in the Preparation of Chiral Auxiliaries:
2-HYDROXYIMINO-2-(PHENYLSULFONYL)ACETONITRILE is employed in the preparation of chiral auxiliaries, which are essential in asymmetric synthesis to induce enantioselectivity. Its use in this capacity aids chemists in obtaining specific enantiomers of chiral molecules, a critical aspect in the development of pharmaceuticals and agrochemicals.
Used in Antioxidant Research:
As a nitroxide radical, 2-HYDROXYIMINO-2-(PHENYLSULFONYL)ACETONITRILE is investigated for its potential as an antioxidant. Research is focused on understanding its role in protecting cells from oxidative stress, which could have implications for the development of therapies to combat various diseases and conditions associated with oxidative damage.
Used in Chemical and Biochemical Research:
Due to its unique properties, 2-HYDROXYIMINO-2-(PHENYLSULFONYL)ACETONITRILE is a valuable tool in chemical and biochemical research. It is used to explore new reaction mechanisms, develop novel synthetic methodologies, and study the behavior of radicals in various chemical systems.

Check Digit Verification of cas no

The CAS Registry Mumber 74755-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,5 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74755-16:
(7*7)+(6*4)+(5*7)+(4*5)+(3*5)+(2*1)+(1*6)=151
151 % 10 = 1
So 74755-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O3S/c9-6-8(10-11)14(12,13)7-4-2-1-3-5-7/h1-5,11H

74755-16-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-2-(benzenesulfonyl)-2-hydroxyiminoacetonitrile

1.2 Other means of identification

Product number -
Other names HMS554M04

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74755-16-1 SDS

74755-16-1Downstream Products

74755-16-1Relevant academic research and scientific papers

Thio and sulfonyl glyoxylnitrileoxime phosphates and phosphonates

-

, (2008/06/13)

Compounds of the formula EQU1 in which R is lower alkyl; R1 is lower alkyl or lower alkoxy; X is thio or sulfonyl; R2 is alkyl, benzothiazolo, benzyl, naphthyl, benzodiazolo-1,3, thiazolo, phenyl or substituted phenyl wherein said substituents are chloro, bromo, methyl or methoxy and the use of these compounds as insecticides.

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