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6134-57-2

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6134-57-2 Usage

Description

Pentane-2,3,4-trione 3-phenylhydrazone is a yellow crystalline solid with the molecular formula C12H12N2O, derived from the reaction of 2,3,4-pentanetrione and phenylhydrazine. It is commonly used in organic synthesis and as a reagent in the preparation of organic compounds, and has been found to exhibit potential biological activities, including antioxidant and antibacterial properties.

Uses

Used in Organic Synthesis:
Pentane-2,3,4-trione 3-phenylhydrazone is used as a reagent in the preparation of organic compounds for its ability to form complexes with a variety of metal ions, enhancing the synthesis process.
Used in Research and Development Laboratories:
Pentane-2,3,4-trione 3-phenylhydrazone is used as a research tool for its ability to form complexes with metal ions, aiding in the study of metal ion interactions and their applications in various fields.
Used in Chemical Sciences:
Pentane-2,3,4-trione 3-phenylhydrazone is utilized in chemical sciences for its potential biological activities, such as antioxidant and antibacterial properties, contributing to the development of new chemical entities with these properties.
Used in Biological Sciences:
In biological sciences, this compound is employed for its potential biological activities, which can be explored for applications in medicine and biotechnology, such as the development of new drugs or antimicrobial agents.

Check Digit Verification of cas no

The CAS Registry Mumber 6134-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6134-57:
(6*6)+(5*1)+(4*3)+(3*4)+(2*5)+(1*7)=82
82 % 10 = 2
So 6134-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O2/c1-8(14)11(9(2)15)13-12-10-6-4-3-5-7-10/h3-7,12H,1-2H3

6134-57-2SDS

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 2,3,4-Pentanetrione, 3-(phenylhydrazone)

1.2 Other means of identification

Product number -
Other names Pentane-2,3,4-trione 3-phenylhydrazone

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:6134-57-2 SDS

6134-57-2Relevant articles and documents

Reversible switching of arylazopyrazole within a metal-organic cage

Hanopolskyi, Anton I.,De, Soumen,Bia?ek, Micha? J.,Diskin-Posner, Yael,Avram, Liat,Feller, Moran,Klajn, Rafal

, p. 2398 - 2407 (2019)

Arylazopyrazoles represent a new family of molecular photoswitches characterized by a near-quantitative conversion between two states and long thermal half-lives of the metastable state. Here, we investigated the behavior of a model arylazopyrazole in the

Chemoproteomics-Enabled De Novo Discovery of Photoswitchable Carboxylesterase Inhibitors for Optically Controlled Drug Metabolism

Dwyer, Brendan G.,Wang, Chao,Abegg, Daniel,Racioppo, Brittney,Qiu, Nan,Zhao, Zhensheng,Pechalrieu, Dany,Shuster, Anton,Hoch, Dominic G.,Adibekian, Alexander

supporting information, p. 3071 - 3079 (2020/12/09)

Herein, we report arylazopyrazole ureas and sulfones as a novel class of photoswitchable serine hydrolase inhibitors and present a chemoproteomic platform for rapid discovery of optically controlled serine hydrolase targets in complex proteomes. Specifica

Mixed isatin with 3-(2-(aryl)hydrazono)acetylacetone mn(ii), co(ii) and ni(ii) complexes: Antibacterial evaluation and molecular properties prediction

Hassan, Ashraf S.

, p. 533 - 541 (2021/02/03)

The metal complexes {Ni (II), Co (II) and Mn (II)} of 3-(2-(aryl)hydrazono)acetylacetone with isatin were synthesized and screened for their in vitro antibacterial activity against four pathogenic microorganisms {two Gram-positive and two Gram negative}.

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