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3-Phenylsydnone, with the molecular formula C14H9NO2, is a yellow crystalline solid that serves as a reagent in organic synthesis. Characterized by its unique ability to engage in photochemical reactions and its potential as a precursor in the synthesis of other organic compounds, 3-Phenylsydnone is a valuable building block in organic chemistry. Its structure and properties have garnered interest for its potential applications in pharmaceuticals and as a photoinitiator in photopolymerization reactions.

120-06-9

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120-06-9 Usage

Uses

Used in Organic Synthesis:
3-Phenylsydnone is used as a reagent for its ability to participate in various organic reactions, contributing to the creation of a wide range of organic compounds due to its unique structural features.
Used in Pharmaceutical Industry:
3-Phenylsydnone is utilized as a precursor in the synthesis of pharmaceuticals, leveraging its potential to be transformed into biologically active molecules for medicinal applications.
Used as a Photoinitiator in Photopolymerization:
In the field of materials science, 3-Phenylsydnone is employed as a photoinitiator to trigger photopolymerization reactions, facilitating the formation of polymers under the influence of light, which is crucial for various industrial applications, including coatings, adhesives, and 3D printing.
Used in Research and Development:
3-Phenylsydnone serves as a subject of study for scientists exploring its photochemical properties and potential uses, further expanding its applications in different areas of chemistry and material science.

Check Digit Verification of cas no

The CAS Registry Mumber 120-06-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 120-06:
(5*1)+(4*2)+(3*0)+(2*0)+(1*6)=19
19 % 10 = 9
So 120-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O2/c11-8-6-10(9-12-8)7-4-2-1-3-5-7/h1-6H/p+1

120-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyloxadiazol-3-ium-5-olate

1.2 Other means of identification

Product number -
Other names 3-Phenylsydnone

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:120-06-9 SDS

120-06-9Upstream product

120-06-9Downstream Products

120-06-9Related news

Selectivity of 1,3-dipolar cycloaddition of methyl propiolate to 3-Phenylsydnone (cas 120-06-9) in near- or supercritical carbon dioxide08/31/2019

The selectivity of the 1,3-dipolar cycloaddition reaction of methyl propiolate to 3-phenylsydnone was measured under various conditions of pressure (7.6–30.4 MPa) and temperature (333–423 K) in near- or supercritical carbon dioxide. The reaction produces a mixture of two regioisomers, 3-carbom...detailed

The sydnone ring as an ortho-director of lithiation. 2.1 Dilithiation of 3-Phenylsydnone (cas 120-06-9) and regiospecific o-aryl acylation using N-methoxy-N-methylamides08/30/2019

Readily available 3-phenylsydnone (1) reacts with n-butyllithium/TMEDA to form the dilithio species 2 which can be regiospecifically acylated at the ortho-aryl position using N-methoxy-N-methylamides (Weinreb's amides).detailed

Cycloadditiion of 3-Phenylsydnone (cas 120-06-9) with cyclooctatetraene08/29/2019

3-Phenylsydnone reacts with cyclooctatetraene to give a 2:1-cycloadduct containing the dihydrobullvalene moiety as the major product.detailed

The sydnone ring as an ortho-director of lithiation. Dilithiation of 3-Phenylsydnone (cas 120-06-9) and trapping by electrophiles08/28/2019

Readily available 3-phenylsydnone (3) reacts with n-butyllithium/TMEDA to form the dilithio species 4 which can be trapped with suitable electrophiles. This represents the first use of a mesoionic ring system for directed lithiation.detailed

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