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2,6-DIMETHYL-4-HYDRAZINOQUINOLINE is a heterocyclic aromatic compound with the molecular formula C11H13N3. It features a quinoline ring system with dimethyl substitutions at the 2 and 6 positions and a hydrazino group at the 4 position.

29125-48-2

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29125-48-2 Usage

Uses

Used in Organic Synthesis:
2,6-DIMETHYL-4-HYDRAZINOQUINOLINE is used as a reagent to introduce the quinoline moiety into various chemical compounds, which is essential for the synthesis of a wide range of organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-DIMETHYL-4-HYDRAZINOQUINOLINE is used as a building block for synthesizing biologically active molecules, contributing to the development of new drugs with potential therapeutic applications.
Used as a Fluorescent Reagent:
2,6-DIMETHYL-4-HYDRAZINOQUINOLINE is also utilized as a fluorescent reagent in biochemical assays, aiding in the detection and analysis of various biomolecules.
Used in Anticancer Research:
2,6-DIMETHYL-4-HYDRAZINOQUINOLINE has been studied for its potential anticancer activities, making it a candidate for further research and development in cancer treatment.
Used in Antiviral Research:
Additionally, 2,6-DIMETHYL-4-HYDRAZINOQUINOLINE has been investigated for its potential antiviral properties, indicating its possible use in the development of antiviral therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 29125-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,2 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29125-48:
(7*2)+(6*9)+(5*1)+(4*2)+(3*5)+(2*4)+(1*8)=112
112 % 10 = 2
So 29125-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N3/c1-7-3-4-10-9(5-7)11(14-12)6-8(2)13-10/h3-6H,12H2,1-2H3,(H,13,14)

29125-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-DIMETHYL-4-HYDRAZINOQUINOLINE

1.2 Other means of identification

Product number -
Other names 4-hydrazino-2,6-dimethylquinoline

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:29125-48-2 SDS

29125-48-2Downstream Products

29125-48-2Relevant academic research and scientific papers

N1-{4-[(10S)-Dihydroartemisinin-10-oxyl]}phenylmethylene-N 2-(2-methylquinoline-4-yl)hydrazine derivatives as antiplasmodial falcipain-2 inhibitors

Luo, Wei,Liu, Yang,Wang, Jian,Guo, Chun,Lu, Wei-Qiang,Cui, Kun-Qiang

, p. 3073 - 3079,7 (2020/08/20)

A series of N1-{4-[(10S)-dihydroartemisinin- 10-oxyl]}phenylmethylene-N2-(2-methylquinoline-4-yl) hydrazine derivatives 9a-9n possessing 4-quinolylhydrazone and artemisinin cores were herein synthesized and evaluated for their activities against cysteine protease falcipain- 2 of Plasmodium falciparum. The structures were clearly confirmed by elemental analysis, 1H NMR, and mass spectra. The pharmacological results indicated that all compounds showed excellent activity against recombinant falcipain-2 (IC50 = 0.15-2.28 μM). The best one of this series was compound 9d (IC50 = 0.15 μM). The molecular docking results showed that the compound 9d made close contact with the key active site of cysteine protease falcipain-2.

Synthesis and some transformations of 6(8)-substituted 4-hydrazino-2- methylquinolines

Avetisyan,Aleksanyan,Ambartsumyan

experimental part, p. 427 - 431 (2010/09/20)

6(8)-Substituted 4-hydrazino-2-methylquinolines were synthesized by reaction of the corresponding 4-chloro-2-methylquinolines with hydrazine hydrate. Reactions of the title compounds with ethyl acetoacetate and acetone gave 2,4-dimethyl-1H-pyrrolo[3,2-c]q

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