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Ethanone, 1-(4-hydrazinophenyl)(9CI) is a chemical compound characterized by the molecular formula C9H11N3O. It is recognized for its hydrazine functional group, which provides a unique reactivity that is instrumental in the synthesis of a variety of organic compounds. Ethanone, 1-(4-hydrazinophenyl)(9CI) is also valued for its potential as a ligand in coordination chemistry, where it can form stable complexes with transition metal ions. Its versatility and reactivity make it a significant player in the field of chemistry, with potential for further research and development across different industries.

62646-10-0

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62646-10-0 Usage

Uses

Used in Pharmaceutical Synthesis:
Ethanone, 1-(4-hydrazinophenyl)(9CI) is utilized as a key intermediate in the synthesis of pharmaceuticals. Its hydrazine functional group allows for the creation of a diverse range of organic compounds, which are essential in the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, Ethanone, 1-(4-hydrazinophenyl)(9CI) is employed as a building block for the synthesis of various agrochemicals. Its reactivity contributes to the development of compounds that can be used in the production of pesticides, herbicides, and other agricultural chemicals.
Used in Coordination Chemistry:
Ethanone, 1-(4-hydrazinophenyl)(9CI) is used as a ligand in coordination chemistry. It forms stable complexes with transition metal ions, which are important in the study of metal coordination and the development of new materials with potential applications in catalysis, sensing, and other areas.
Overall, Ethanone, 1-(4-hydrazinophenyl)(9CI) is a versatile chemical compound with a broad spectrum of applications in the chemical industry, pharmaceuticals, agrochemicals, and coordination chemistry, showcasing its potential for future research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 62646-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,4 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62646-10:
(7*6)+(6*2)+(5*6)+(4*4)+(3*6)+(2*1)+(1*0)=120
120 % 10 = 0
So 62646-10-0 is a valid CAS Registry Number.

62646-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-hydrazinylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 4-acetylphenylhydrazine

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:62646-10-0 SDS

62646-10-0Relevant academic research and scientific papers

Visible-light-mediated phosphonylation reaction: formation of phosphonates from alkyl/arylhydrazines and trialkylphosphites using zinc phthalocyanine

Hosseini-Sarvari, Mona,Koohgard, Mehdi

supporting information, p. 5905 - 5911 (2021/07/12)

In this work, we developed a ligand- and base-free visible-light-mediated protocol for the photoredox syntheses of arylphosphonates and, for the first time, alkyl phosphonates. Zinc phthalocyanine-photocatalyzed Csp2-P and Csp3-P bond formations were efficiently achieved by reacting aryl/alkylhydrazines with trialkylphosphites in the presence of air serving as an abundant oxidant. The reaction conditions tolerated a wide variety of functional groups.

Synthesis and antimicrobial activity of 3-(substituted-phenyl)-sydnones

Moustafa,Eisa

, p. 397 - 401 (2007/10/02)

3-(3 or 4-Acetylphenyl)-sydnones 7, 8 have been synthesized by formation of the glycines 3, 4, followed by nitrosation to 5, 6 and cyclization with acetic anhydride to sydnones. Sydnone derivatives carrying chalcone moieties 15, 16 were prepared by format

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